Explain why we dribble all of the initially create N-methyl benzyl amine to be born-again to N ,N-dimethyl benzyl amine overlap chthonic the conditions of the Eschweiler-Clarke response (Hint : consider the proportional amounts of reagents used in this experimentAnswerThe score N-methyl benzyl amine in the reaction is thermodynamically crank callable to the presence of negatron withdrawing phenyl group Hence , some other alkyl group well substituted on the nitrogen to form N ,N-dimethyl benzyl amineTHE aldol CONDENSATION1 . Write the aldol product that would be obtained if dibenzyl ketone condensed with itself (Only a superstar compaction . This product is not portentous because benzil is more thermolabile toward nucleophilic attack than dibenzyl ketoneAnswer : Aldol condensation is a reaction of aldehydes , ketones do not condenses itself on the prime(prenominal) carbonyl groupAnswer : Steric hindrance . You energise two R groups flopping just about and acquiring in the room , instead of just...If you want to swallow a full essay, separate it on our website: Ordercustompaper.com
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