
justify why we expect all of the initially formed N-methyl benzyl amine to be reborn to N ,N-dimethyl benzyl amine product under the conditions of the Eschweiler-Clarke response (Hint : consider the relative amounts of reagents use in this experimentAnswerThe formed N-methyl benzyl amine in the reaction is thermodynamically unstable callable to the presence of electron withdrawing phenyl group Hence , a nonher alkyl group easily substituted on the nitrogen to form N ,N-dimethyl benzyl amineTHE ALDOL CONDENSATION1 . carry through the aldol product that would be obtained if dibenzyl ketone condensed with itself (Only a single ejection seat . This product is not grandiloquent because benzil is more reactive toward nucleophilic contend 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 acquiring in the way , instead of just...If you want to get a full essay, order it on our website: Orderessay
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