(SYN) Show how to synthesize each of these alcohols from a ketone or aldehyde that has the same number of carbons as the alcohol. (a) OH (b) HO (c) OH
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- (a) (b) HO N N-H Catalytic H+ (-H₂O) ? (c) NH2 HO N (d)Draw the structure of each of the following molecules. (a) cyclohexyl butanoate; (b) 1,1-dimethylethyl hexanoate; (c) phenyl 4,4-dinitroheptanoateFor the generic ester RC(O)OR′, which bond will hydrolyzeunder basic conditions?(a) the R¬C bond (b) the C“O bond (c) the C¬O bond(d) the O¬R′ bond (e) more than one of the above
- 6) Which is the organic product for the following reaction? (a) (b) (c) (d) LOH OH COOH OH OH COOH COOH KMnO4 H₂O (e) None of the above products will be formed(a) Provide the structures of two possible organic products. (b) Circle the major organic product. NBS hv1. Give the IUPAC names for the following alcohols. (a) OH OH (b) ОН (c) HO CH3CHCH2CHCHCH3 CH2CH2CCH3 -CH3 CH3 CH3 CH3 (d) (e) (f) CH3 HO HO OH
- GIVE IUPAC NAMES FOR THE FOLLOWING STRUCTURES: (a) (b) СНО (c) H-C-OH CH2OH *CH3 (d) (e) (f) CHO OH | || CH3CHCH2CH CH3CHCCH2CH3 CH3 ОНСdetermine the major organic product in addition to identifying the wheather it is racemic.|| CH2-С-NH 2 KOBr → (A); Product (A) is : C-0- CH3 (a) (b) (c) NH (d) NH 3.