Explain why we expect all of the initially formed N-methyl benzyl amine to be regenerate to N ,N-dimethyl benzyl amine product under the conditions of the Eschweiler-Clarke response (Hint : consider the relative amounts of reagents used in this experimentAnswerThe formed N-methyl benzyl amine in the reaction is thermodynamically unstable due to the presence of electron withdrawing phenyl group Hence , another alkyl group easily substituted on the nitrogen to form N ,N-dimethyl benzyl amineTHE A LDOL CONDENSATION1 . Write the aldol product! that would be obtained if dibenzyl ketone condensed with itself (Only a single condensation . This product is not dreadful because benzil is more reactive toward nucleophilic attack than dibenzyl ketoneAnswer : Aldol condensation is a reaction of aldehydes , ketones do not condenses itself on the first carbonyl groupAnswer : Steric hindrance . You have two R groups flopping around and acquiring in the way , instead of just...If you want to get a full essay, order it on our website: OrderEssay.net
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