Homework Answers
Question.6.Ans :- Structure (I) i.e. Option (a) is the answer.
The given reaction is Bimolecular nucleophilic substitution (SN2) mechanism because N3- is a stronger nucleophile and DMSO is the polar aprotic solvent. In SN2 mechanism backside attack of nucleophile occurs on substrate through which configuration of products changes i.e. invert.
Therefore, option (a) is the answer.
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14) When (R)-2-bromobutane reacts with Cl2/hw, which of the following is true CH3 CH3 H--C1 CH3 CH3 A) Only I is formed. B) Only II is formed. C) I and II are formed in equal amounts. D) I and II are formed in unequal amounts. E) I and II could never form under these conditions. 15) Which of the following compounds is more stable? Explain. -CHb. 16) Give the best product for the reaction. CH CH:CH Br, ight 17) Complete...
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