5 - tad‘\ethQ PrWLm-u CM€WM NM'4‘“[V bUfi-QN...

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Unformatted text preview: tad‘ \ethQ PrWLm-u CM€WM NM '4‘“: [V bUfi-QN qg’q-3’1SMGH)00\§964 cwe‘f’fw‘w NM AflQeweS "' 1 26 CHAPTER 4 0 INTRODUCTION TO ALKENES. STRUCTURE AND REACTIVITY ref-molecular I fiflIBONDINQ- energy'_OEisulgted .2P;_orl5i_tals._ ' clearan- ' occupanc -' ._ ._ ._m_'__ ' - .-..isdlatedf2_pz_ - ._ _ ' atomic orbital . ' - __ 3.;3 isolated 2p: ' _.._atomiciorbital _. filer Bi... _ -_7rrnolecular_orbital - BONDING nuclear position Figure 4.6 An orbital interaction diagram showing the overlap of 2p orbitals to form bonding and antibonding 1.- molecular orbitals of ethylene.The 1r bond is formed when two electrons occupy the bonding vrmolecular orbital. Wave peaks and wave troughs are shown with different colors.The nodal planes are perpendicular to the page. noMW P (‘M ~43 2 WV 1) CMOOR Owe; (MM? diuth 3) new; '5 VIM/MW Su‘asi‘fl‘ue‘q‘s a VW‘H «MyI Brcfi:w3— um VI 4009 Mid—2 0) ?~\d~\m -\-Rw- \ a (9sz S. “c 3 q “1%.. A: lc= C'\"1 H' g E‘ \'O\’V‘W\g— l- \- “Mm ...
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5 - tad‘\ethQ PrWLm-u CM€WM NM'4‘“[V bUfi-QN...

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