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rationalise 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 employ in this experimentAnswerThe formed N-methyl benzyl amine in the reception is thermodynamically unstable callable to the presence of electron withdrawing phenyl group Hence , another alkyl group easily substituted on the nitrogen to form N ,N-dimethyl benzyl amineTHE ALDOL CONDENSATION1 . economize the aldol product that would be obtained if dibenzyl ketone condensed with itself (Only a single abridgment . This product is not awful because benzil is more reactive toward nucleophilic round down than dibenzyl ketoneAnswer : Aldol condensation is a reaction of aldehydes , ketones do not condenses itself on the first carbonylic groupAnswer : Steric hindrance . You have two R groups flopping around and getting in the way , instead of just...If you want to get a full essay, order it on our website: Ordercustompaper.com
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