(a)
Interpretation:
From the given
Concept Introduction:
An E2 reaction is a concerted, one-step reaction in which the proton and the halide ion are removed in the same step.
A strong base favours an E2 reaction. A high concentration of a base favours an E2 reaction. If one of the reactants is charged, an E2 reaction will be favoured by the least polar solvent that will dissolve the reactant. If neither of the reactant is charged an E2 reaction is favoured by the protic polar solvent. The major product is a stable
(b)
Interpretation:
From the given alkyl halides undergoes E2 reaction has to be identified.
Concept Introduction:
An E2 reaction is a concerted, one-step reaction in which the proton and the halide ion are removed in the same step. A strong base favours an E2 reaction. A high concentration of a base favours an E2 reaction. If one of the reactants is charged, an E2 reaction will be favoured by the least polar solvent that will dissolve the reactant. If neither of the reactant is charged an E2 reaction is favoured by the protic polar solvent.
The major product is a stable alkene, unless the reactants are sterically hindered.
(c)
Interpretation:
From the given alkyl halides undergoes E2 reaction has to be identified.
Concept Introduction:
An E2 reaction is a concerted, one-step reaction in which the proton and the halide ion are removed in the same step. A strong base favours an E2 reaction. A high concentration of a base favours an E2 reaction. If one of the reactants is charged, an E2 reaction will be favoured by the least polar solvent that will dissolve the reactant. If neither of the reactant is charged an E2 reaction is favoured by the protic polar solvent.
The major product is a stable alkene, unless the reactants are sterically hindered.

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Chapter 8 Solutions
Essential Organic Chemistry, Global Edition
- Provide the reagents for the following reactions.arrow_forwardIf I have 1-bromopropene, to obtain compound Z, I have to add two compounds A1 and A2. Indicate which compounds are needed. P(C6H5)3arrow_forwardDraw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side product is continuously removed to drive the reaction toward products. O CH3CH2NH2, TSOH Select to Draw >arrow_forward
- Indicate the products obtained by reacting fluorobenzene with a sulfonitric mixture.arrow_forwardIf I have 1-bromopropene, to obtain compound A, I have to add NaOH and another compound. Indicate which compound that would be. C6H5 CH3arrow_forwardIf I have 1-bromopropene and I want to obtain (1,1-dipropoxyethyl)benzene, indicate the compound that I should add in addition to NaOH.arrow_forward
- Draw the major product of this reaction. Ignore inorganic byproducts. Ο HSCH2CH2CH2SH, BF3 Select to Draw I Submitarrow_forwardFeedback (7/10) Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side product is continuously removed to drive the reaction toward products. Incorrect, 3 attempts remaining Ο (CH3CH2)2NH, TSOH Select to Draw V N. 87% Retryarrow_forwardIf I want to obtain (1,1-dipropoxyethyl)benzene from 1-bromopropene, indicate the product that I have to add in addition to NaOH.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning

