1.Which compound will the most stable carbocation in an Sn1 reactions? 2.When a
ID: 856721 • Letter: 1
Question
1.Which compound will the most stable carbocation in an Sn1 reactions?
2.When a substrate undergoes an Sn1 reaction, the reaction proceed with?
3.Which alkyl halide reacts the fastest by the Sn2 mechanism?
4.Which compound shown is the major product formed when the solvolysis of 2-iodo-3-methylpentane in CH3OH proceeds with a hydride shift?
6.Which of the following carbocations will be the most stable and most likely carbocation formed during the solvolysis of 1-chloro-2-methylcyclohexane in CH3OH?
7.Which product will be formed in the Sn2 reaction shown below?
8.When a substrate undergoes an Sn2 reaction, the reaction proceeds with?
9.Which alkyl bromide reacts the fastest with Ch3OH by the Sn1 mechanism?
10.Which of the following carbocations will be the most stable likely carbocation formed during the solvolysis of 2-bromo-3,3-dimethylpentane in Ch3OH?
12.Which two diastereomeric products will be formed in the solvolysis reaction shown below?
13.Identify the rate determining step in the Sn1 reaction shown below?
14.which alkyl halide undergoes an Sn2 reaction with sodium cyanide at the fastest rate?
15.Which halide ion reacts the fastest with CH3CH2X via an Sn2 Mechanism?
16.What does the 2 in Sn2 refer to?
17.What does the 1 in sn1 refer to?
18.Which of the following shown below will be the most likely product formed as the result of an alkyl shift during the solvolysis of 1-iodo-2,-2dimethylpentane in Ch3OH?
19.Which compound will be formed in the Sn2 reaction shown below?
20.What product will be formed in the Sn2 reaction shown below?
1.Which compound will the most stable carbocation in an Sn1 reactions? 2.When a substrate undergoes an Sn1 reaction, the reaction proceed with? 3.Which alkyl halide reacts the fastest by the Sn2 mechanism? 4.Which compound shown is the major product formed when the solvolysis of 2-iodo-3-methylpentane in CH3OH proceeds with a hydride shift? 6.Which of the following carbocations will be the most stable and most likely carbocation formed during the solvolysis of 1-chloro-2-methylcyclohexane in CH3OH? 7.Which product will be formed in the Sn2 reaction shown below? 8.When a substrate undergoes an Sn2 reaction, the reaction proceeds with? 9.Which alkyl bromide reacts the fastest with Ch3OH by the Sn1 mechanism? 10.Which of the following carbocations will be the most stable likely carbocation formed during the solvolysis of 2-bromo-3,3-dimethylpentane in Ch3OH? 12.Which two diastereomeric products will be formed in the solvolysis reaction shown below? 13.Identify the rate determining step in the Sn1 reaction shown below? 14.which alkyl halide undergoes an Sn2 reaction with sodium cyanide at the fastest rate? 15.Which halide ion reacts the fastest with CH3CH2X via an Sn2 Mechanism? 16.What does the 2 in Sn2 refer to? 17.What does the 1 in sn1 refer to? 18.Which of the following shown below will be the most likely product formed as the result of an alkyl shift during the solvolysis of 1-iodo-2,-2dimethylpentane in Ch3OH? 19.Which compound will be formed in the Sn2 reaction shown below? 20.What product will be formed in the Sn2 reaction shown below?Explanation / Answer
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