The following article will add knowledge about “Identify all of the McLafferty rearrangement products of N-ethyl 2-methylpentanamide“. Let’s keep an eye on the content below!

Question: Identify all of the McLafferty rearrangement products of N-ethyl 2-methylpentanamide

Identify all of the McLafferty rearrangement products of N-ethyl 2-methylpentanamide:

Select one or more:

• a. ethene (ethylene)
• b. propene
• c. ionized 2-methylpentenamide (in tautomeric form)
• d. ionized N-ethyl propanamide (in tautomeric form)
• e. ionized N-ethyl 2-methylpropenamide (in tautomeric form)
• f. pentene
• g. ionized 2-methylpentanamide (in tautomeric form)

Anwer

Draw the substitution products for each of the following reactions; if the products can exist as stereoisomers, show what stereoisomers are obtained:

a. (R) – 2 -bromopentane +CH₃O⁻+CH₃O⁻ 

b. (R)−3 -bromo- 3 -methylheptane +CH₃OH 

c. benzyl chloride +CH₃CH₂OH+CH₃CH₂OH 

d. allyl chloride +CH₃OH+CH₃OH 

e. 1 -bromo- 2 -butene +CH₃O⁻+CH₃O⁻ 

f. 1 -bromo- 2 -butene +CH₃OH+CH₃OH

Last words

Above is the solution of “Identify all of the McLafferty rearrangement products of N-ethyl 2-methylpentanamide“. If you have good solutions or comments, please leave a message.