Rathodex1KEY - / CHEM 239 Name: Test 1, Version C First...

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Unformatted text preview: / CHEM 239 Name: Test 1, Version C First Last April 18, 2007 1. For each of the following starting materials and sequence of reaction treatments, PROVIDE A STRUCTURE OF THE MOST LIKELY REACTION PRODUCT (15 points). 4. For each of the following starting materials and sequence of reaction treatments, r PROVIDE A STRUCTURE OF THE MOST LIKELY REACTION PRODUCT (15 POINTS). 2. Provide an acceptable name for the following 5 compounds (30 points) : 3 ' HSJ r0¥319WtOIlo ac; J I _ . 3‘ _ o g r I 14,! rp Z/wo/arofama/E, 6M- _. a was 3'0 ‘I: CHEM 239 Name: Test 1, Version B First. Last April 18, 2007 - ‘1. Provide a detailed description of the mechanism underlying ACID catalyzed hydrolysis of an AMIDE (20 points) . H 0 - a“ H (Z) , H [7 I if} l Q/wm P [3/ mm” ' ’le K . :§—H H I1 5» H \ «7 v @ 85H &\,, N (33 o H /'\A;.Q’Q” I I :1 Fr“; ‘ éfl_‘ R /I\nm a I V 0 ll / .. A’ (9 fix :O—N V I 63 Du H “ l Q/(Li‘an (L "Ty: ‘_ g] 0’ H, ' (J - /fi\ + AI] / l2" 0-14 K OH /' 1'4 ' I H Lag/4.1“3 . .7 cameo-l PVOJMJS .4) II/o mt'bfifl/Gd wwws a.) fll/ GAG/f: 41.4 Carrfog le'o'wjg / '5. Outline! an efficient synthesis strategy for the following compounds based on what you have learned in ' Chapters 19-21 (20 points): ' ' ' ~ *** use readily available simple aldehydes, ketones, esters, and alkyl halides *** m envuxavmmn l A . umwmm News“ mm... x. D 0 0 mat/Eton ,___. ‘7 /\0)\ 'DA +-~a / \..__\\D ‘Ng’ .m— b / \ ‘DA ...
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Rathodex1KEY - / CHEM 239 Name: Test 1, Version C First...

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