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A) Which alkyl halide will produce only one alkene product when heated with sodi

ID: 1017157 • Letter: A

Question

A) Which alkyl halide will produce only one alkene product when heated with sodium methoxide in methanol?

a) 2-chloro-4-methylpentane b) 2-chloro-3-ethylpentane c) 3-chloro-2-methylpentane d) 2-chloro-2-methylpentane e) 3-chloro-3-ethylpentane

B) When (2S,3R)-2-bromo-3-methylpentane undergoes reaction with sodium methoxide in methanol, the product is

a) (E)-3-methyl-2-pentene b) 2-methyl-1-pentene c) 3-methyl-1-pentene d) (Z)-3-methyl-2-pentene e) 2-methyl-2-pentene

C) Which alkene is the major product when 2-bromo-2-methylpentane is heated with potassium tert-butoxide in tert-butanol?

a) (Z)-2-methyl-3-pentene b) 2-methyl-4-pentene c) (E)-2-methyl-3-pentene d) 2-methyl-2-pentene e) 2-methyl-1-pentene

D) When (1R,2S)-1-bromo-2-methylcyclohexane is heated with sodium methoxide in methanol, the major product is

a) (S)-3-methylcyclohexene b) (S)-4-methylcyclohexene c) (R)-3-methylcyclohexene d) (R)-4-methylcyclohexene e) 1-methylcyclohexene

E) When the compound shown below undergoes E1 elimination, base-abstraction of a hydrogen ion from the initially formed carbocation forms the minor product

F) When the compound shown below undergoes E1 elimination, the initially formed carbocation undergoes a hydride shift to preferentially form

G) When (2S,3R)-2,3-dibromohexane undergoes reaction with sodium iodide in acetone, the product is

a) (E)-3-hexene b) 1-hexene c) (Z)-2-hexene d) (Z)-3-hexene e) (E)-2-hexene

H) When the compounds shown below undergoes E1 elimination, the initially formed carbocation undergoes a hydride shift to preferentially form a second carbocation. Methoxide base-abstraction from this second carbocation forms the products

I) Which alkene is the major product when 2-bromo-2-methylpentane is heated with sodium ethoxide in ethanol?

a) (Z)-2-methyl-3-pentene b) 2-methyl-4-pentene c) 2-methyl-2-pentene d) (E)-2-methyl-3-pentene e) 2-methyl-1-pentene

J) When (2S,3S)-2-bromo-3-methylpentane undergoes reaction with sodium methoxide in methanol, the product is

a) (E)-3-methyl-2-pentene b) (Z)-3-methyl-2-pentene c) 2-methyl-1-pentene d) 3-methyl-1-pentene e) 2-methyl-2-pentene

Explanation / Answer

a- answer is e.

If see the structure of the molecule i have make the carbon in bold which are going to eliminate will give the same single product

CH3CH2ClC(CH2CH3)CH2CH3

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