Final_D_key - F'inC-JL. - A Nomenclature ( 0% points) _...

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Unformatted text preview: F'inC-JL. - A Nomenclature ( 0% points) _ Please provide an accepiable IUF’AC name iorthe folfowmg compounds. E) "'3 “A axemc—afi 0 .. q, 0 I I i 2. m3 3 M were - Awmmg/ [94:42me Br E/H ‘7me 2w elfihtxawi 3. L 7b 43¢; 3. Reactions (7 points each, total: 35 points) Please give the major product, or necessary reagents, or starting material for each of the following reactions in the box provided. Be sure your drawing indicates the relative orientation of the substiments (1.3., stereochemistry) in the molecuie. w : <11 4; ‘ . ‘ L -- / w-‘r 2 4,." am w Psi. M“? N6 > 3h Aria :11. CHEEHCI O n ' 1. SOCIQ —————-—-——-——3-- 4_ (GH30H2)2GHCOH 2. (CHAJi’Cul-j 1352911039 I 1 2 5. CHacHchecHon 2. 5H3 THF ’ ./\/\r* H ‘ . 3- H3 . L) ' (Note: THF - teirahydmi‘u ran ' 5H G \“2 . J H / ,MOH T7 c. MECHA mu : {1 8 points) _ Provide a detailed step-by—step mechanism for the transformation below. Draw 31! intermediates and show movement of elf e1ectrons with “curved arrows". CH3 ,5 W" “9 gig/CH wea- 6- a) k2“ , .z . ME” 27% F/Qéfibax flea/255% «:5:— Speotrosoopy (1 0 points) Molecuie 3; whose formula is C10H15N hasthe foliowing IR, 1H NMR and 13C NMB spectra (see next page "A"; in the 1H NMR spectrum the numbers above (near) {he signals refer to the relative proten integration ratios. Please give the stmcture of a in the box provided. E. Synthésis :(18 points) Starting withgfienzeng, any one or two carbon alcohol. and any inorganic reagents. synthesize the following compound: {\DCH-i '1" CRT? I (a ...
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Final_D_key - F'inC-JL. - A Nomenclature ( 0% points) _...

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