Solutions_Manual_for_Organic_Chemistry_6th_Ed 128

Solutions_Manual_for_Organic_Chemistry_6th_Ed 128 - (c) ny...

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6-52 continued (b) (i) · 0: H ( H H equivalent resonance foNs H H } . ±" H h (iV) ± H2 h equivaLent resonance foNs i 1/±· .J²,} loss oF bromiDe gIVes unstahle 10 carhoCaT±o² I±aT qu³Ck´y rEARaNg²S to a 2° aµµyµ³C carboCA¶IOn equ³valent resonanCe Fo·s-saMe as FroM parT (³³³¸
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Unformatted text preview: (c) ny one substitutIon prodUct arises froM equIvalent resonance foNs. (i) (iiI OCHCH3 653 cis + trans Mos stable al\YLic (+ o 3 and 2 C) (Ii (Iv) OCHCH3 saMe as part (iII) cis + trans + >0 aLYlic + on 1 ad 2 C) 12 least sable...
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This note was uploaded on 02/27/2010 for the course CHEM 140 taught by Professor Wade during the Spring '10 term at Whitman.

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