Would appreciate help on questions 32,33,34 and 35. Thank you in
advance!
32. What is the predicted product of the reaction shown? 1. DMSO, (COCI)₂ 1-hexanol 2. Et3N A. hexanal B. hexanoic acid C. 2-hexanone D. 2-chlorohexane E. 1-hexanol 33. Compound A on ozonolysis yields the two products shown. What is the structure of compound A? Compound A 1.03 2. (CH₂)₂S Ju a IV A. B. II C. III D. IV E. none of these 34. Which of the following compounds is least reactive towards a nucleophilic addition reaction? I 11 III IV I A. I B. II III D. IV E. V 35. Which of the following statements is consistent with the mechanism for the nucleophilic addition of aldehydes/ketones under basic conditions? A. a proton transfer followed by a nucleophilic attack B. a nucleophilic attack followed by a proton transfer C. nucleophilic attack is the only step proton transfer is not required D. 36. A compound with two OH groups attached to the same carbon is known as A. an acetal a hemiacetal a hydrate a vicinal hydrate none of these E. 37. A compound with two OR groups attached to the same carbon is known as A. an acetal B. a hemiacetal C. a hydrate D. a vicinal hydrate E. none of these ABCDE C. ABCDE B. C. D.
Would appreciate help on questions 32,33,34 and 35. Thank you in advance!
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