Question

5. Show how the following reaction would proceed. NH2 1.) NaNO2, HCI 2.) H2O Nucleophilic Substitution Product Elimination Pr

1.) Fill in the missing reagents or products, and show the mechanism of formation, where applicable. (a) (b) o 1.) DIBAL-H (-

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Answer #1

5. Diazotization gives diazonium salt which then loose N2 to form elimination product and Substitution product.

Wolff kishnner Reduction( N2H4/KOH) convert ketone into alkane.

DiBALH convert the ester(lactone) into aldehyde and alcohol.

Nucleophilic addition of HCN gives caynohydrin.NH2 Nanor/H + Elimindion substi tution NrHu/EOH DI BAL-HI a t H HT CN

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