Solved

The Conversion of Alkyl Azides into Primary Amines Through a Procedure

Question 2

Essay

The conversion of alkyl azides into primary amines through a procedure called the Staudinger reaction is shown.
The conversion of alkyl azides into primary amines through a procedure called the Staudinger reaction is shown. The mechanism of the first part of the reaction is conceptually similar to the Wittig reaction that we've talked about, where an ylide reacts with a carbonyl to yield an oxaphosphetane, which then rearranges to an alkene and triphenylphosphine oxide. Provide an arrow pushing mechanism for the first part of the Staudinger reaction, the reaction of triphenylphosphine (TPP) and an alkyl azide to produce an iminophosphorane and nitrogen gas. The mechanism of the first part of the reaction is conceptually similar to the Wittig reaction that we've talked about, where an ylide reacts with a carbonyl to yield an oxaphosphetane, which then rearranges to an alkene and triphenylphosphine oxide.
The conversion of alkyl azides into primary amines through a procedure called the Staudinger reaction is shown. The mechanism of the first part of the reaction is conceptually similar to the Wittig reaction that we've talked about, where an ylide reacts with a carbonyl to yield an oxaphosphetane, which then rearranges to an alkene and triphenylphosphine oxide. Provide an arrow pushing mechanism for the first part of the Staudinger reaction, the reaction of triphenylphosphine (TPP) and an alkyl azide to produce an iminophosphorane and nitrogen gas. Provide an arrow pushing mechanism for the first part of the Staudinger reaction, the reaction of triphenylphosphine (TPP) and an alkyl azide to produce an iminophosphorane and nitrogen gas.
The conversion of alkyl azides into primary amines through a procedure called the Staudinger reaction is shown. The mechanism of the first part of the reaction is conceptually similar to the Wittig reaction that we've talked about, where an ylide reacts with a carbonyl to yield an oxaphosphetane, which then rearranges to an alkene and triphenylphosphine oxide. Provide an arrow pushing mechanism for the first part of the Staudinger reaction, the reaction of triphenylphosphine (TPP) and an alkyl azide to produce an iminophosphorane and nitrogen gas.

Correct Answer:

verifed

Verified

Related Questions

Q1: Identify the missing reagent for the reaction.<br>

Q3: Provide a detailed, arrow-pushing mechanism for the

Q4: Predict the major organic product in the

Q5: Two students working in a laboratory are

Q6: Identify the missing reagent for the reaction.<br>

Q7: Deduce the structure of the missing starting

Q8: For each pair of reactions, circle "faster"

Q9: Outline a synthesis to achieve this transformation.<br>

Q10: Predict the major organic product of the

Q11: Treatment of a mixture of cyclopentanone (A)