tag:blogger.com,1999:blog-55994565391130012632024-03-13T14:16:40.287-07:00KIMIA ORGANIK 1Anonymoushttp://www.blogger.com/profile/11883815665246551426noreply@blogger.comBlogger3125tag:blogger.com,1999:blog-5599456539113001263.post-15441601216736535052012-11-02T08:44:00.001-07:002012-11-10T07:20:47.939-08:00<span id="goog_936684372"></span><span id="goog_936684373"></span><br />
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<b><span style="font-family: "Times New Roman","serif"; font-size: 12pt; line-height: 115%;"> REAKSI-REAKSI
OKSIDATIF PADA HIDROKARBON DAN REAKSI-REAKSI ASAM BASA SENYAWA ORGANIK<o:p></o:p></span></b></div>
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<b><span style="font-family: "Times New Roman","serif"; font-size: 18pt; line-height: 115%;"> REAKSI-REAKSI
OKSIDATIF PADA HIDROKARBON<o:p></o:p></span></b></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;"> Reaksi
Oksidasi juga disebut terbakar reaksi. Oksidasi yang tidak lengkap ditandai
dengan nyala api merah<o:p></o:p> dan ada jelaga. Jelaga terbakar
atom.<o:p></o:p>Hanya
beberapa bagian dari senyawa alkena dan alkuna yang terbakar sepenuhnya.Hal ini
disebabkan oleh atom karbon yang lebih tinggi dalam alkena dan alkuna dari yang
di alkana.Hasil karbon yang lebih tinggi lebih banyak oksigen diperlukan untuk
membakar.<o:p></o:p></span></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Contoh:<o:p></o:p></span></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;"><o:p> </o:p>Oksidasi besi (II) menjadi besi
(III) dengan hidrogen peroksida dalam kehadiran asam:<o:p></o:p></span></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Fe2+ → Fe3+ + e− <o:p></o:p></span></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">H2O2 + 2 e− → 2 OH− <o:p></o:p></span></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Keseluruhan persamaan: <o:p></o:p></span></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">2 Fe2+ + H2O2 + 2 H+ → 2 Fe3+ + 2
H2O<o:p></o:p></span></div>
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<!--[if !supportLists]--><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">1.<span style="font-family: "Times New Roman"; font-size-adjust: none; font-size: 7pt; font-stretch: normal; font-style: normal; font-variant: normal; font-weight: normal; line-height: normal;"> </span></span><!--[endif]--><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Oksidasi pada Alkana<o:p></o:p></span></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Reaksi Oksidasi pada Senyawa
Hidrokarbon, Suatu senyawa alkana yang bereaksi dengan oksigen menghasilkan
karbon dioksida dan air disebut dengan reaksi pembakaran. Perhatikan persamaan
reaksi oksidasi pada senyawa hidrokarbon berikut. <o:p></o:p></span></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Reaksi pembakaran tersebut, pada
dasarnya merupakan reaksi oksidasi. Pada senyawa metana (CH4) dan karbon
dioksida (CO2) mengandung satu atom karbon. Kedua senyawa tersebut harus
memiliki bilangan oksidasi nol maka bilangan oksidasi atom karbon pada senyawa
metana adalah –4, sedangkan bilangan oksidasi atom karbon pada senyawa karbon
dioksida adalah +4. Bilangan oksidasi atom C pada senyawa karbon dioksida
meningkat (mengalami oksidasi), sedangkan bilangan oksidasi atom C pada senyawa
metana menurun.<o:p></o:p></span></div>
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<!--[if !supportLists]--><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">2.<span style="font-family: "Times New Roman"; font-size-adjust: none; font-size: 7pt; font-stretch: normal; font-style: normal; font-variant: normal; font-weight: normal; line-height: normal;"> </span></span><!--[endif]--><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Oksidasi pada Alkena: Hidroksilasi
dan Pemutusan Ikatan<o:p></o:p></span></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Hidroksilasi AlkenaMerupakan peristiwa adisi gugus –OH
pada kedua karbonikatan rangkap. Dapat terjadi dengan mereaksikan alkenadengan
osmium tetroksida. Reaksi terjadi secara<o:p></o:p></span></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Syn
stereokimia dan menghasilkan 1,2-dialkohol, atau disebut diol.<o:p></o:p></span></div>
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<a href="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEjLC5KIfowVwr-b_lpfsSGvsNcTzGPRuSKPQxo49FYh-GgDIJJ6xi2nkGMpehE8dmnqf7oPOn9U-EM8cItqDu8n-KCqYHCGN9pQH5w2oRbzjyShm5I7qUQN67nRdOQRlXVzCDiPLH6IHaqD/s1600/Image602.jpg" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><img border="0" height="240" src="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEjLC5KIfowVwr-b_lpfsSGvsNcTzGPRuSKPQxo49FYh-GgDIJJ6xi2nkGMpehE8dmnqf7oPOn9U-EM8cItqDu8n-KCqYHCGN9pQH5w2oRbzjyShm5I7qUQN67nRdOQRlXVzCDiPLH6IHaqD/s320/Image602.jpg" width="320" /></a></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;"><o:p> </o:p>Hidroksilaksi
alkena tidak melibatkan pembentukanintermediet karbokation tetapi
intermedietcyclic osmate yang terbentuk dalam satu tahap adisi OSO4 pada
alkena.Cyclic osmat ini kemudian dipecah menggunakan sodiumbisulfat (NaHSO3).<o:p></o:p></span></div>
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<b><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Oksidasi
dengan Ozonolisis<o:p></o:p></span></b></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Untuk reaksi ozonolisis, pasti akan terjadi pemutusan
rantai. Pemutusan Ikatan pada alkena, Pada pembahasan sebelumnya, reaksi adisi
pada alkena akan menghasilkan pemutusan salah satu ikatan rangkappada alkena
menghasilkan produk dengan karbon yangsemula berikatan rangkap menjadi ikatan
tunggal.Akan tetapi, dengan menggunakan oksidator yang sangat kuat akan dapat
memutus kedua ikatan dalam ikatanrangkap alkena.Ozon (O3) biasanya digunakan
untuk memecah ikatanrangkap dalam alkena. Ozon dapat mengadisi dengan cepat
pada alkena membentuk intermediet molozonideyang dengan cepat pula mengalami
penataan ulangmembentuk ozonida. Ozonida kemudian diperlakukandengan reduktor
seperti logam zinc dalam asam asetatuntuk mengubahnya menjadi senyawa karbonil.
Hasil akhir ozonolisis adalah pecahnya ikatan rangkap C=C dan digantikan dengan
ikatan rangkap dengan oksigen.<o:p></o:p></span></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Contoh
reaksi:</span></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Reaksi ini dibagi menjadi 2, yaitu ozonolisis reduktif
dan oksidatif.<o:p></o:p></span></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Dari gambar diatas, dapat kita simpulkan untuk reaksi
ozonolisis reduktif (Zn, H<sub>2</sub>O) akan menghasilkan produk hingga
tingkat karbonil saja (Aldehid dan Keton) sedangkan untuk reaksi ozonolisis
oksidatif (H<sub>2</sub>O<sub>2</sub>) akan menghasilkan produk hingga tingkat
asam karboksilat jika memungkinkan.<o:p></o:p></span></div>
<div style="color: black; text-align: justify;">
</div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Sebagai
tambahan, perlu anda ketahui bahwa ozon adalah zat reaktif yang bersifat
karsogenik.<o:p></o:p></span></div>
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<span class="style34">Pembakaran
alkuna melibatkan reaksi antara alkuna dengan oksigen. Reaksi ini bersifat
eksotermik. Sama halnya dengan alkena,Jika alkuna dibakar dengan oksigen
berlebih maka pembakaran akan berlangsung dengan sempurna dan menghasilkan C</span><span class="style21">O</span><span class="style41">2</span><span class="style34"> dan H</span><span class="style41">2</span><span class="style34">O.</span></div>
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2C<sub>2</sub>H<sub>2(g)</sub> +5O<sub>2(g)</sub>
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<br />
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Klasifikasi asam-basa pada senyawa
organik pada umumnya mengikuti teori asam-basa Bronsted –Lowry. Penentuan
kekuatan asam-basa dapat dilihat dari arga pKa atau pKb nya. Yang perlu diingat
bahwa asam kuat akan menghasilkan basa konjugasi yang stabil, begitu juga
sebaliknya akan lebih kompleks. Kebanyakan asam adalah netral, maka basa
konjugasi dari sebagian besar asam bermuatan negatif, karena asam tersebut
kehilangan proton. </div>
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<b>Asam organik</b></div>
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Asam organik dicirikan oleh adanya atom
hidrogen yang terpolarisasi positif. Terdapat dua macam asam organik, yang
pertama adanya atom hidrogen yang terikat dengan atom oksigen, seperti pada
metil alkohol dan asam asetat. Kedua, adanya atom hidrogen yang terikat pada
atom karbon di mana atom karbon tersebut berikatan langsung dengan gugus
karbonil (C=O), seperti pada aseton. </div>
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Metil alkohol mengandung ikatan O-H dan
karenanya bersifat asam lemah, asam asetat juga memiliki ikatan O-H yang
bersifat asam lebih kuat. Asam asetat bersifat asam yang lebih kuat dari metil
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Keasaman aseton diperlihatkan dengan basa
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<b>Basa Organik</b></div>
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Basa organik dicirikan dengan
adanya atom dengan pasanganelektron bebas yang dapat mengikat proton.
Senyawa-senyawa yangmengandung atom nitrogen adalah salah satu contoh
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tergantung lingkungannya. Misalnya aseton dan metil alkohol dapat bertindak
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Amina adalah
suatu senyawa yang mengandung gugusan amino. Gugusan amino<span style="letter-spacing: -0.75pt;">mengandung nitrongen terikat kepada satu sampai
tiga atom karbon (tetapi bukan gugusankarbonil) dan sejumlah atom hidrogen
(tidak ada, satu atau dua). Apabila salah satu karbon</span>yang terikat pada
atom nitorgen adalah karbon karbonil, senyawanya adalah amida, bukan<span style="letter-spacing: -0.75pt;">amina.</span>Amina sangat penting dalam biokimia.
Misalnya serotonin, suatu senyawa yang<span style="letter-spacing: -0.75pt;">didapat
dalam sistem susunan saraf, mengirimkan impuls saraf dan mengerutkan
pembuluhdarah. Histamin adalah senyawa yang bertanggung jawab pada gejala
alergi.</span><o:p></o:p></span></div>
<br />
<div>
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; text-align: justify;">
<br /></div>
<br />
<div style="text-align: justify;">
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Reaksi dari
Amina<o:p></o:p></span></div>
<br />
<div style="text-align: justify;">
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;"> A. Asilasi<o:p></o:p></span></div>
<br />
<div style="text-align: justify;">
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: 0.75pt;">Asilasi berarti substitusi dengan suatu gugusan asil. Asilasi nukleofilik
dari suatu</span><span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: -0.75pt;">amina, dimana aminanya kehilangan proton mendapatkan gugusan asil,
menghasilkan suatuamida</span><span style="font-family: "Times New Roman","serif"; font-size: 12pt;"><o:p></o:p></span></div>
<br />
<div style="text-align: justify;">
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; text-align: justify;">
<span class="a"><span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: -0.5pt; line-height: 115%;">Senyawa yang
bereaksi dengan amina menghasilkan amida adalah ester, asam anhidrid,</span><span style="word-spacing: 4px;">dan asam halide. Asam </span></span><span class="l7"><span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: -0.5pt; line-height: 115%;">halide adalah yang paling reaktif dari ketiganya Karen
asam </span></span><span class="l6"><span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: -0.5pt; line-height: 115%;">halide</span></span><span class="a"><span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: 0.5pt; line-height: 115%;"><span style="word-spacing: 10px;">mem</span></span><span class="l8"><span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: 0.5pt; line-height: 115%;">pun</span></span><span class="l6"><span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: 0.5pt; line-height: 115%;">yai gugus</span></span><span class="l7"><span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: 0.5pt; line-height: 115%;">an
yang mening</span></span><span class="l6"><span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: 0.5pt; line-height: 115%;">galkan
terbaik</span></span><span class="l7"><span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: 0.5pt; line-height: 115%;">, sedang</span></span><span class="l6"><span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: 0.5pt; line-height: 115%;">kan ester adal</span></span><span class="l7"><span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: 0.5pt; line-height: 115%;">ah yan</span></span><span class="l6"><span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: 0.5pt; line-height: 115%;">g paling</span></span></span><span class="a"><span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: -0.5pt; line-height: 115%;"><span style="word-spacing: 1px;">kurang reaktif</span><o:p></o:p></span></span></div>
<br />
<div style="text-align: justify;">
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: -0.5pt;">Asam nitrit mengalami berbagai reaksi dengan berbagai macam amina.</span><span style="font-family: "Times New Roman","serif"; font-size: 12pt;"><o:p></o:p></span></div>
<br />
<div style="text-align: justify;">
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<b><span style="font-family: "Times New Roman","serif"; font-size: 12pt;"> <i>Alkil
amina tersier <o:p></o:p></i></span></b></div>
<br />
<div style="text-align: justify;">
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;"> bereaksi
dengan asam nitrit menghasilkan garam amina, seperti <span style="letter-spacing: -0.5pt;">terjadi dengan asam apa saja.</span><o:p></o:p></span></div>
<br />
<div style="text-align: justify;">
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<b><i><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Aril amina
tersier <o:p></o:p></span></i></b></div>
<br />
<div style="text-align: justify;">
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: 0.5pt;">mengalami reaksi substitusi aromatic elektrofilik menghasilkan</span><span style="font-family: "Times New Roman","serif"; font-size: 12pt;"> senyawa nitroso<span style="letter-spacing: -0.5pt;">, suatu senyawa yang mengandung guggusan nitroso
–N=O<o:p></o:p></span></span></div>
<br />
<div style="text-align: justify;">
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<b><i><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Ami
sekunder <o:p></o:p></span></i></b></div>
<br />
<div style="text-align: justify;">
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt; letter-spacing: 0.5pt;">bereaksi dengan asam nitri menghasilkan N-nitrosoamina, biasanya</span><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">disebut nitrosamine, senyawa dengan
gugusan nitroso terikat kepada nitrogen dari amina.<span style="letter-spacing: -0.5pt;">Banyak senyawa yang mengandung gugusan N-nitroso telah dibuktikan
karsinogenik pada</span> bintang dalam laboratorium.<o:p></o:p></span></div>
<br />
<div style="text-align: justify;">
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<b><i><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Alkil amina
primer <o:p></o:p></span></i></b></div>
<br />
<div style="text-align: justify;">
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;"> bereaksi
dengan asam nitrit membnetuk <o:p></o:p></span></div>
<br />
<div style="text-align: justify;">
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;"> garam
alkyl diazonium, R – N = N Cl-. Garam ini tidak stabil, kehilangan
nitrogen (N2, suatu gugusan meninggalkanterbaik), dan menghasilkan karbokation
yang tidak stabil ini kemudian mengalami reaksi<span style="letter-spacing: -0.5pt;">substitusi dan eliminasi menghasilkan campuran hasil reaksi.</span><o:p></o:p></span></div>
<br />
<div style="text-align: justify;">
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<b><i><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Aril amina
primer <o:p></o:p></span></i></b></div>
<br />
<div style="text-align: justify;">
</div>
<br />
<div class="MsoNormal" style="background-color: #f3f3f3; line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">juga
bereaksi dengan asam nitrit menghasilkan garam diazonium.Reaksi ini adalah yang
paling penting dari reaksi asam nitrit. Tidak seperti garam alkyldiazonium,
garam aril diazonium relative stabil jika disimpan dalam keadaan dingin.
Jikalarutan campuran reaksi dibiarkan menjadi hangat, ion diazoniumnya bereaksi
dengan air <span style="letter-spacing: -0.5pt;">membentuk suatu fenol.</span><o:p></o:p></span></div>
<div class="MsoNormal" style="background-color: #f3f3f3; line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;"><o:p><br /></o:p></span><!--[if gte mso 10]>
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<div style="background-color: #f3f3f3; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Permasalahan 1 :<o:p></o:p></span></div>
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adisi pada alkena akan menghasilkan pemutusan salah satu ikatan rangkap pada
alkena menghasilkan produk dengan karbon yangsemula berikatan rangkap menjadi
ikatan tunggal. Akan tetapi, dengan menggunakan oksidator yang sangat kuat akan
dapat memutus kedua ikatan dalam ikatan rangkap alkena.Ozon (O3) biasanya
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cepat pada alkena membentuk intermediet molozonide yang dengan cepat pula
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Anonymoushttp://www.blogger.com/profile/11883815665246551426noreply@blogger.com5tag:blogger.com,1999:blog-5599456539113001263.post-73022781604390016672012-10-19T04:50:00.000-07:002012-10-20T14:23:26.208-07:00<link href="file:///C:%5CUsers%5CCOMPAQ%5CAppData%5CLocal%5CTemp%5Cmsohtmlclip1%5C01%5Cclip_filelist.xml" rel="File-List"></link><link href="file:///C:%5CUsers%5CCOMPAQ%5CAppData%5CLocal%5CTemp%5Cmsohtmlclip1%5C01%5Cclip_themedata.thmx" rel="themeData"></link><link href="file:///C:%5CUsers%5CCOMPAQ%5CAppData%5CLocal%5CTemp%5Cmsohtmlclip1%5C01%5Cclip_colorschememapping.xml" rel="colorSchemeMapping"></link><!--[if gte mso 9]><xml>
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<div class="MsoNormal">
<b><span style="font-family: "Times New Roman","serif"; font-size: 20pt; line-height: 115%;">REAKSI-REAKSI
ORGANIK<o:p></o:p></span></b></div>
<div class="MsoNormal" style="line-height: normal;">
<b><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">1. <i>Reaksi Oksidasi pada Senyawa Hidrokarbon</i></span></b><b><i><span style="font-family: "Times New Roman","serif"; font-size: 12pt;"><o:p></o:p></span></i></b></div>
<div class="MsoNormal" style="line-height: normal;">
<span style="font-family: "Times New Roman","serif";">Reaksi
Oksidasi adalah reaksi pengikatan oksigen oleh suatu zat.Sumber oksigen pada
reaksi oksidasi disebut oksidator. Oksidator yang paling banyak digunakan
adalah udara (02), tetapi dapat juga senyawa yang mudah melepaskan oksigen.
Contoh senyawa oksidator antara lain: kalium klorat (KC10J, kalium permanganat
(KMnOJ, hidrogen peroksida (H202), asam nitrat (HN03), dan asam sulfat pekat
(H2S04).<o:p></o:p></span></div>
<div class="MsoNormal" style="line-height: normal;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Suatu
senyawa alkana yang bereaksi dengan oksigen menghasilkan karbon dioksida dan
air disebut dengan reaksi pembakaran. Perhatikan persamaan reaksi oksidasi pada
senyawa hidrokarbon berikut.<o:p></o:p></span></div>
<div class="MsoNormal" style="line-height: normal;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">CH<sub>4(g)</sub>
+ O<sub>2(g)</sub> → CO<sub>2(g)</sub> + H<sub>2</sub>O<sub>(g)</sub><o:p></o:p></span></div>
<div class="MsoNormal" style="line-height: normal; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Reaksi pembakaran tersebut, pada dasarnya merupakan
reaksi oksidasi. Pada senyawa metana (CH<sub>4</sub>) dan karbon dioksida (CO<sub>2</sub>)
mengandung satu atom karbon. Kedua senyawa tersebut harus memiliki bilangan
oksidasi nol maka bilangan oksidasi atom karbon pada senyawa metana adalah –4,
sedangkan bilangan oksidasi atom karbon pada senyawa karbon dioksida adalah +4.<o:p></o:p></span></div>
<div class="MsoNormal" style="line-height: normal; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Bilangan oksidasi atom C pada senyawa karbon dioksida
meningkat (mengalami oksidasi), sedangkan bilangan oksidasi atom C pada senyawa
metana menurun.<o:p></o:p></span></div>
<div class="MsoNormal" style="line-height: normal;">
<b><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">2. <i>Reaksi Adisi pada Senyawa Hidrokarbon</i></span></b><b><span style="font-family: "Times New Roman","serif"; font-size: 12pt;"><o:p></o:p></span></b></div>
<span style="font-family: 'Times New Roman',serif; font-size: 12pt; line-height: 200%;">Reaksi adisi adalah
reaksi pemutusan ikatan rangkap (pengubahan ikatan rangkap menjadi
ikatan kovalen tunggal ). Reaksi adisi antara lain dapat digunakan
untuk membedakan <b>alkana</b> dengan <b>alkena</b>. <b>Reaksi</b> pengenalan ini dilakukan dengan penambahan <b>bromine</b> (Br<sub>2</sub>) yang berwarna merah coklat. Terjadinya reaksi adisi ditandai dengan hilangmya warna merah coklat daro <b>bromin</b> (Br<sub>2</sub>). Karena alkana tidak memiliki ikatan rangkap ( tidak mengalami reaksi adisi adisi ) warna merah dari bromin tidak berubah.<o:p></o:p></span><br />
<span style="font-family: 'Times New Roman',serif; font-size: 12pt; line-height: 200%;">Dalam
suatu reaksi adisi suatu alkena, ikatan pi terputus dan pasangan
elektronnya digunakan untuk membentuk dua ikatan sigma baru. Dalam tiap
kasus, <b>atom karbon sp</b><sup><b>2</b> </sup>direhibridisasi menjadi sp<sup>3</sup>.
Senyawa yang mengandung ikatan pi biasanya berenergi lebih tinggi
daripada senyawa yang sepadan yang mengandung hanya ikatan sigma; oleh
karena itu reaksi adisi biasanya eksoterm.</span>Reaksi adisi hanya dapat
terjadi pada senyawa yang memiliki ikatan rangkap seperti <i><b><u>alkena dan alkuna</u></b></i>.<b> </b>Alkena dan alkuna dapat mengalami
reaksi adisi dengan hidrogen, halogen maupun asam halida (HX).<br />
<br />
<span style="font-family: 'Times New Roman',serif; font-size: 12pt; line-height: 200%;"></span><br />
<b>Reaksi Adisi Alkuna oleh Hidrogen</b><br />
Reaksinya dapat digambarkan secara umum sebagai berikut.<br />
<div class="separator" style="clear: both; text-align: center;">
<a href="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEiYmyQNNtA4cEQDq-aoCDku_ncZYvfny-03LX-VVrHIKSwULtliVKundkJjDOdLFSPTbTw2ive7Jbam6_x6CIJZTih92iPLE0KLDiKGqjDMLtEX72XjkPFdjUYuCu8cftUIlPuM-FKvVtkR/s1600/reaksi+adisi+alkuna.PNG" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><img border="0" height="113" src="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEiYmyQNNtA4cEQDq-aoCDku_ncZYvfny-03LX-VVrHIKSwULtliVKundkJjDOdLFSPTbTw2ive7Jbam6_x6CIJZTih92iPLE0KLDiKGqjDMLtEX72XjkPFdjUYuCu8cftUIlPuM-FKvVtkR/s320/reaksi+adisi+alkuna.PNG" width="320" /></a></div>
<br />
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<div class="MsoNormal" style="line-height: normal; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Jika senyawa karbon memiliki ikatan rangkap dua
(alkena) atau rangkap tiga (alkuna) dan pada atom-atom karbon tersebut
berkurang ikatan rangkapnya, kemudian digantikan dengan gugus fungsi (atom atau
molekul). Reaksi tersebut dinamakan reaksi adisi. Perhatikan reaksi
antara 1-propena dengan asam bromida menghasilkan 2-bromopropana sebagai
berikut.</span></div>
<div class="separator" style="clear: both; text-align: center;">
<a href="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhLC9ufkH9OSsn1Ls5ZDPn_3QiywD6sR4BkClrayE48fDKqFtbMCZvT8U95aZKTrUVE8dTRshUzvYmrc5OtAsFs2frv0_G1rUKm5yJjgl11NRYFvslJK7F1UKgv-mSCq5qC8g2JqDMnMLXm/s1600/reaksi-adisi.jpg" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><img border="0" height="66" src="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhLC9ufkH9OSsn1Ls5ZDPn_3QiywD6sR4BkClrayE48fDKqFtbMCZvT8U95aZKTrUVE8dTRshUzvYmrc5OtAsFs2frv0_G1rUKm5yJjgl11NRYFvslJK7F1UKgv-mSCq5qC8g2JqDMnMLXm/s320/reaksi-adisi.jpg" width="320" /></a></div>
<div class="MsoNormal" style="line-height: normal; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;"><o:p></o:p></span></div>
<div class="MsoNormal" style="line-height: normal;">
<br /></div>
<div class="MsoNormal" style="line-height: normal; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Hidrokarbon yang memiliki ikatan rangkap dua atau
rangkap tiga merupakan senyawa tak jenuh. Pada senyawa tak jenuh ini
memungkinkan adanya penambahan atom hidrogen. Ketika suatu senyawa tak jenuh
direaksikan dengan hidrogen halida maka akan menghasilkan produk tunggal.<o:p></o:p></span></div>
<div class="MsoNormal" style="line-height: normal; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Aturan Markovnikov: adisi asam terhadap alkena yang
tak simetri, atom H akan mengikat atom H lebih banyak.<o:p></o:p></span></div>
<div class="MsoNormal" style="line-height: normal;">
<b><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">3. <i>Reaksi Substitusi pada Senyawa Hidrokarbon</i></span></b><b><span style="font-family: "Times New Roman","serif"; font-size: 12pt;"><o:p></o:p></span></b></div>
<div class="MsoNormal" style="line-height: normal; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Reaksi substitusi merupakan reaksi penggantian gugus
fungsi (atom atau molekul) yang terikat pada atom C suatu senyawa hidrokarbon.
Pada reaksi halogenasi alkana, atom hidrogen yang terikat pada atom C senyawa
alkana digantikan dengan atom halogen. Ketika campuran metana dan klorin
dipanaskan hingga 100°C atau radiasi oleh sinar UV maka akan dihasilkan senyawa
klorometana, seperti reaksi berikut.<o:p></o:p></span></div>
<div class="MsoNormal" style="line-height: normal;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">CH<sub>4(g)</sub>
+ Cl<sub>2(g)</sub> →
CH<sub>3</sub>Cl<sub>(g)</sub> + HCl<sub>(g)</sub><o:p></o:p></span></div>
<div class="MsoNormal" style="line-height: normal;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Jika gas
klorin masih tersedia dalam campuran, reaksinya akan berlanjut seperti berikut.<o:p></o:p></span></div>
<div class="MsoNormal" style="line-height: normal;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">CH<sub>3</sub>Cl<sub>(g)</sub>
+ Cl<sub>2(g)</sub> </span><span style="font-family: "Cambria Math","serif"; font-size: 12pt;"></span><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">→ CH<sub>2</sub>Cl<sub>2(g)</sub>
+ HCl<sub>(g)</sub><o:p></o:p></span></div>
<div class="MsoNormal" style="line-height: normal;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">CH<sub>2</sub>Cl<sub>2(g)</sub>
+ Cl<sub>2(g)</sub> </span><span style="font-family: "Cambria Math","serif"; font-size: 12pt;"></span><span style="font-family: "Times New Roman","serif"; font-size: 12pt;"> → CHCl<sub>3(g)</sub>
+ HCl<sub>(g)</sub><o:p></o:p></span></div>
<div class="MsoNormal" style="line-height: normal;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">CHCl<sub>3(g)</sub>
+ Cl<sub>2(g)</sub> </span><span style="font-family: "Cambria Math","serif"; font-size: 12pt;"></span><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">→ CCl<sub>4(g)</sub>
+ HCl<sub>(g)</sub><o:p></o:p></span></div>
<div class="MsoNormal" style="line-height: normal; text-align: justify;">
<br /></div>
<div class="MsoNormal" style="line-height: normal;">
<b><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">4. <i>Reaksi Eliminasi pada Senyawa Hidrokarbon</i></span></b><b><span style="font-family: "Times New Roman","serif"; font-size: 12pt;"><o:p></o:p></span></b></div>
<div class="MsoNormal" style="line-height: normal; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Reaksi eliminasi </span><span style="font-family: "Times New Roman","serif";">merupakan
reaksi peruraian suatu molekul menjadi molekul-molekul lain di mana salah satu
molekul dikatakan tereliminasi. Reaksi eliminiasi dapat juga dikatakan sebagai
reaksi pembentukan ikatan rangkap dari ikatan tunggal (kebalikan dari reaksi
adisi).<o:p></o:p></span></div>
<div class="MsoNormal" style="margin-bottom: 0.0001pt;">
<i><span style="font-family: "Times New Roman","serif";">Reaksi
eliminasi H<sub>2</sub> dari alkana menjadi alkena</span></i><span style="font-family: "Times New Roman","serif";"> <o:p></o:p></span></div>
<div class="MsoNormal">
<span style="font-family: "Times New Roman","serif";">CH<sub>3</sub>
- CH<sub>2</sub> - CH<sub>3</sub> --> CH<sub>3</sub> - CH = CH<sub>2</sub> +
H<sub>2</sub><br />
<sub> </sub> <o:p></o:p></span></div>
<div class="MsoNormal">
<i><span style="font-family: "Times New Roman","serif";">Reaksi eliminasi air (dehidrogenasi) dari alkohol</span></i><span style="font-family: "Times New Roman","serif";"> <o:p></o:p></span></div>
<div class="MsoNormal">
<span style="font-family: "Times New Roman","serif";">Alkohol
dapat bereaksi membentuk alkena dengan bantuan katalis H<sub>2</sub>SO<sub>4</sub>
pekat berlebih pada suhu 180<sup>o</sup>C. <o:p></o:p></span></div>
<div class="MsoNormal">
<span style="font-family: "Times New Roman","serif";">CH<sub>3</sub>
- CH<sub>2</sub> - OH --> CH<sub>2</sub> = CH<sub>2</sub> + H<sub>2</sub>O<o:p></o:p></span></div>
<div class="MsoNormal" style="line-height: normal; margin-bottom: 0.0001pt;">
<i><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Reaksi eliminasi HX dari haloalkana (dehidrohalogenasi) </span></i><span style="font-family: "Times New Roman","serif"; font-size: 12pt;"><o:p></o:p></span></div>
<div class="MsoNormal" style="line-height: normal; margin-bottom: 0.0001pt;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Haloalkana R
- X dapat bereaksi dengan gugus - OH yang larut dalam alkohol seperti NaOH
etanolis atau CH<sub>3</sub>OK, membentuk alkuna. <o:p></o:p></span></div>
<div class="MsoNormal">
<br /></div>
<div class="MsoNormal" style="line-height: normal; text-align: justify;">
<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Masalah :<o:p style="font-family: inherit;"></o:p></span></div>
<div class="MsoNormal" style="font-family: inherit;">
Dalam reaksi adisi, molekul senyawa yang mempunyai ikatan rangkap
menyerap atom atau gugus atom sehingga ikatan rangkap berubah menjadi
ikatan tunggal. <span style="font-size: 12pt; line-height: 115%;">Saya pernah membaca bahwa </span>Senyawa benzena sukar mengalami
reaksi adisi. Padahal, senyawa benzena memiliki ikatan rangkap ? mengapa hal
tersebut bisa terjadi? kemudian saya ada membaca literatur bahwa reaksi benzena umumnya melalui reaksi substitusi, walaupun ada sebagian reaksi yang melalui reaksi adisi. bagaimana mekanisme reaksi benzena mengalami reaksi adisi?<link href="file:///C:%5CUsers%5CCOMPAQ%5CAppData%5CLocal%5CTemp%5Cmsohtmlclip1%5C01%5Cclip_filelist.xml" rel="File-List"></link><link href="file:///C:%5CUsers%5CCOMPAQ%5CAppData%5CLocal%5CTemp%5Cmsohtmlclip1%5C01%5Cclip_themedata.thmx" rel="themeData"></link><link href="file:///C:%5CUsers%5CCOMPAQ%5CAppData%5CLocal%5CTemp%5Cmsohtmlclip1%5C01%5Cclip_colorschememapping.xml" rel="colorSchemeMapping"></link><!--[if gte mso 9]><xml>
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Anonymoushttp://www.blogger.com/profile/11883815665246551426noreply@blogger.com5tag:blogger.com,1999:blog-5599456539113001263.post-65219550417028175532012-10-11T07:38:00.000-07:002012-10-20T14:35:36.705-07:00<br />
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<b><span style="font-family: "Times New Roman","serif"; font-size: 16pt; line-height: 115%;">HIDROKARBON
AROMATIK</span></b></div>
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<br /></div>
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<b><span style="font-family: "Times New Roman","serif"; font-size: 16pt; line-height: 115%;"></span></b></div>
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<b><span style="font-family: "Times New Roman","serif"; font-size: 16pt; line-height: 115%;"></span></b></div>
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<b><span style="font-family: "Times New Roman","serif"; font-size: 16pt; line-height: 115%;"></span></b></div>
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<b><span style="font-family: "Times New Roman","serif"; font-size: 16pt; line-height: 115%;"></span></b></div>
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<b><span style="font-family: "Times New Roman","serif"; font-size: 16pt; line-height: 115%;"></span></b></div>
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<b><span style="font-family: "Times New Roman","serif"; font-size: 16pt; line-height: 115%;"></span></b></div>
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<b><span style="font-family: "Times New Roman","serif"; font-size: 16pt; line-height: 115%;"></span></b></div>
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<b><span style="font-family: "Times New Roman","serif"; font-size: 16pt; line-height: 115%;"></span></b></div>
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<b><span style="font-family: "Times New Roman","serif"; font-size: 16pt; line-height: 115%;"></span></b></div>
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<b><span style="font-family: "Times New Roman","serif"; font-size: 16pt; line-height: 115%;"><o:p></o:p></span></b></div>
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<b><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">hidrokarbon
aromatik </span></b><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">merupakan </span><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">hidrokarbon dengan ikatan tunggal dan
atau ikatan ganda di antara atom-atom karbonnya. Konfigurasi 6 atom karbon pada
senyawa aromatik dikenal dengan </span><span style="font-family: "Times New Roman","serif";"><a href="http://id.wikipedia.org/wiki/Benzena" title="Benzena"><span style="color: black; font-size: 12pt; text-decoration: none;">cincin</span></a> benzena</span><span style="font-family: "Times New Roman","serif"; font-size: 12pt;">. Hidrokarbon aromatik dapat berupa <i>monosiklik</i>
atau <i>polisiklik</i>.</span><span style="font-family: "Times New Roman","serif"; font-size: 12pt;"> Senyawa
hidrokarbon aromatik, meliputi; benzena, toluen, etil benzen, xylen(sebagai
BTEX), fenol dan kresol. Senyawa – senyawa ini berbasiskan pada gugusan cincin
yang tersusun oleh enam atom karbon. Senyawa aromatik ditandai dengan sifat ikatan
antar atom karbon dalam cincin, yaitu ikatan tunggal dan ikatan ganda. <o:p></o:p></span></div>
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<span style="font-family: "Times New Roman","serif"; font-size: 12pt;">Struktur
utama senyawa aromatik yang menjadi dasar sifat-sifat kimianya adalah cincin
benzena. Cincin benzena biasa digambarkan sebagai segi-enam beraturan dengan
tiap sudut ditempati oleh atom C yang mengikat satu atom H dan ikatan rangkap
yang berselang-seling antara dua atom C yang berurutan (lihat gambar di bawah
ini). Gambaran ini sempat menguasai senyawa aromatik untuk beberapa puluh tahun
sebelum akhirnya diubah karena sifat-sifat utama ikatan rangkap tidak tampak
pada gambaran struktur benzena sebelumnya. Hidrokarbon aromatik banyak pula
terdapat dalam minyak bumi.</span><span style="font-family: "Times New Roman","serif";">
Contoh senyawa hidrogen aromatik sebagai berikut :</span></div>
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<div style="text-align: justify;">
Hidrokarbon aromatik, senyawa yang mengandung
paling tidak satu cincin benzena. Senyawa heterosiklik yang mencakup atom-atom
nonkarbon dalam struktur cincinnya dan polimer molekul rantai panjang gugus
berulang. Benzena (C<sub>6</sub>H<sub>6</sub>) adalah hidrokarbon induk dari
senyawa yang sangat stabil yang dikenal sebagai senyawa aromatik. Dalam
benzena, menyiratkan struktur yang sangat tak jenuh. Misalnya, bandingkan
jumlah hidrogennya dengan heksana, C<sub>6</sub>H<sub>14</sub>, atau
sikloheksana C<sub>6</sub>H<sub>12</sub>, yang keduanya memiliki enam karbon
tetapi jenuh.</div>
<div style="text-align: justify;">
Meskipun rumus molekulnya demikian, benzena pada
umumnya tidak berperilaku seperti senyawa tak jenuh. Misalnya, senyawa ini
tidak menghilangkan warna larutan bromin seperti layaknya alkena dan alkuna,
atau mudah dioksidasi oleh kalium permanganat. Benzena juga tidak menjalani
reaksi adisi yang khas untuk alkena atau alkuna. Sebaliknya, reaksi utama
benzena ialah substitusi. Contohnya bila diolah dengan bromin dengan bantuan
feri bromida sebagai katalis, benzena menghasilkan bromobenzena dan hidrogen
bromida.</div>
<div style="text-align: justify;">
Menurut
Friedrich August Kekule, Jerman (1865), struktur Benzena dituliskan sebagai
cincin dengan enam atom karbon yang mengandung tiga buah ikatan tunggal dan
tiga buah ikatan rangkap yang berselang seling. Benzena tidak sama dengan
bensin. Benzena merupakan senyawa golongan aromatik dikenal aromatik karena
berbau sedap, sedangkan bensin merupakan campuran senyawa alkana. </div>
<div style="text-align: justify;">
Tatanama Benzena yaitu : monosubstitusi (satu
sustituen), disubstitusi (dua substituen) dan polisubstitusi (lebih dari dua
substituen). Benzena mudah disubstitusi, Reaksi substitusi pada Benzena
diantaranya substitusi aromatik elektrofilik. Substitusi pertama terdiri dari
Halogenasi, Nitrasi, Sulfonasi, Alkilasi dan Asilasi.Substitusi kedua, yaitu
Benzena monosubstitusi mengalami lagi substitusi, sehingga menghasilkan
disubstitusi, dimana produk disubstitusi tergantung pada substituen pengarah
orto,meta dan para.</div>
<div style="text-align: justify;">
<br /></div>
<b>Tatanama Senyawa Aromatik</b><br />
<br />
<u><o:p></o:p></u><br />
<div style="margin-left: 38.25pt; text-indent: -18pt;">
<!--[if !supportLists]--><b><i>a.<span style="font-family: "Times New Roman"; font-size-adjust: none; font-size: 7pt; font-stretch: normal; font-style: normal; font-variant: normal; font-weight: normal; line-height: normal;">
</span></i></b><!--[endif]--><i><b>Tata
nama satu substituen</b></i><b><i><o:p></o:p></i></b></div>
Cl
OH
CH<sub>3 </sub><br />
Kloro benzena
Hidroksi
benzena
Metil benzena<br />
Fenil
klorida
Fenil
alkohol
Toluen<br />
Fenol<br />
NO<sub>2 </sub>NH<sub>2</sub><br />
Nitro benzena Amino benzena<br />
Fenil Amina<br />
Anilina<br />
<br />
<div style="margin-left: 38.25pt; text-indent: -18pt;">
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</span></i></b><!--[endif]--><i><b>Tata
nama dua substituen</b></i><b><i><o:p></o:p></i></b></div>
<div style="text-align: justify;">
Dua atom H pada cincin benzena diganti oleh dua
atom atau gugus atom. Jika substituen letaknya berdekatan di C no.1 dan 2
dinamakan posisi orto. Jika substituen letaknya terhalang oleh satu atom C
dinamakan posisi meta (atom C di No. 1 dan 3) Jika substituen letaknya
terhalang oleh dua atom C dinamakan posisi para (atom C di no.1 dan 4).</div>
<div style="text-align: justify;">
Hanya satu monobromobenzena atau monoklorobenzena
yang pernah diisolasi; artinya tidak ada isomer yang diperoleh dari kedua
reaksi tersebut. Ini menyiratkan bahwa keenam hidrogen pada benzena mestinya
setara secara kimia. Hidrogen manapun yang digantikan oleh bromin, kita
memperoleh monobromobenzena yang sama. </div>
<div style="text-align: justify;">
Teori orbital, juga bermanfaat dalam menjelaskan
struktur benzena. Setiap atom karbon pada benzena hanya berhubungan dengan tiga
atom lain (dua karbon dan satu hidrogen). Jadi, setiap atom karbon
terhibridisasi sp2, seperti pada etilena. Dua orbital sp2 pada setiap atom
karbon bertumpang-tindih dengan orbital yang serupa dari atom karbon
disebelahnya membentuk ikatan sigma pada cincin heksagonal. Orbital sp2 yang
ketiga dari setiap karbon bertumpang-tindih dengan orbital 1s dari hidrogen
membentuk ikatan sigma. Tegak lurus pada bidang yang dibentuk oleh tiga orbital
sp2 pada setiap karbon terdapat orbital p yang mengandung satu elektron, yaitu
elektron valensi keempat. Orbital p pada keenam atom karbon dapat
bertumpang-tindih secara lateral membentuk orbital pi yang menciptakan satu
cincin atau awan elektron diatas dan di bawah bidang cincin. Bangun cincin
benzena dari enam karbon terhibridisasi sp2 ditampilkan secara skematis pada gambar
dibawah ini. Model ini menjelaskan tentang keplanaran benzena.</div>
<div style="text-align: justify;">
Hidrogenasi ikatan rangkap karbon-karbon
merupakan reaksi eksotermik. Banyaknya energi (kalor) yang dilepas ialah
sekitar 26 sampai 30 kkal/mol untuk setiap ikatan rangkap. Nilai tepatnya bergantung
pada substituen yang melekat pada ikatan rangkap. Bila dua ikatan rangkap dalam
suatu molekul dihidrogenasi, besar kalor yang dilepaskan adalah dua kalinya,
dan seterusnya.</div>
<div style="text-align: justify;">
Pada benzena, dapat diketahui bahwa beberapa
substituen (misalnya OH dan CH3) mempercepat reaksi, dan substituen lain (Cl
dan NO2) menghalangi reaksi. Kita tahu dari bukti lain bahwa gugus hidroksil
dan metil lebih bersifat pendonor elektron dibandingkan hidrogen, sedangkan
gugus kloro dan nitro lebih bersifat penarik elektron dibandingkan dengan
hidrogen.</div>
<div style="text-align: justify;">
Pengamatan ini juga mendukung mekanisme
elektrofilik pada substitusi. Jika laju reaksi bergantung pada serangan
elektrofilik artinya pencari elektron pada cincin aromatik, maka substituen
yang bersifat pendonasi elektron ke cincin akan meningkatkan rapatan
elektronnya, dan dengan demikian mempercepat reaksi, substituen yang bersifat
menarik elektron dari cincin akan menurunkan rapatan elektron dalam cincin dan
dengan begitu memperlambat reaksi. Pola reaktivitas ini tepat seperti yang
teramati, tidak saja dengan nitrasi tetapi juga dengan semua reaksi substitusi
aromatik elektrofilik. Suatu substituen dianggap sebagai pengaktif (aktivating)
jika lajunya lebih cepat dan pendeaktif (deactivating) jika lajunya lebih
lambat daripada reaksinya pada benzena.</div>
<div style="text-align: justify;">
Dalam semua gugus pengarah meta, atom berhubungan
dengan cincin membawa muatan positif penuh atau parsial dan dengan demikian
akan menarik elektron dari cincin. Semua pengarah meta dengan demikian juga
merupakan gugus pendeaktif cincin. Sebaliknya, gugus pengarah orto, para pada
umumnya memasuk elektron ke cincin dan dengan demikian merupakan pengaktif
cincin. Pada halogen (F, Cl, Br, dan I) kedua efek yang berlawanan ini
mengakibatkan pengecualian pada aturan tersebut. Karena bersifat sebagai
penarik elektron kuat, halogen merupakan pendeaktif cincin, namun karena adanya
pasangan elektron bebas, maka halogen ialah pengarah orto, para. Sejumlah besar
senyawa dapat dibuat dari zat-zat dengan cincin benzena yang digabungkan. Yang
paling terkenal dari senyawa semacam ini adalah naftalena, yang digunakan dalam
kamper. Senyawa ini dan banyak senyawa serupa lainnya terdapat dalam aspal
cair. Beberapa senyawa dengan beberapa cincin merupakan karsinogen yang
kuat-senyawa tersebut dapat menyebabkan kanker pada manusia dan binatang.<br />
<br />
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Tatanama Benzena yaitu : monosubstitusi (satu
sustituen), disubstitusi (dua substituen) dan polisubstitusi (lebih dari dua
substituen).dapatkan anda membantu saya untuk menjelaskan bagaimana tatanama benzena seperti di atas?<br />
<span style="font-family: "Times New Roman","serif";"><o:p></o:p></span><br />
<span style="font-family: "Calibri","sans-serif"; font-size: 11pt; line-height: 115%;"> </span>
<br />
<div style="text-align: justify;">
<br /></div>
<br />
<span style="font-family: "Times New Roman","serif";"></span><span style="font-family: "Times New Roman","serif"; font-size: 12pt; line-height: 115%;"><o:p></o:p></span><br />
<br />
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<br /></div>
<div class="MsoNormal" style="line-height: normal; margin-bottom: 0.0001pt; text-align: justify;">
<br /></div>
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