(a)
Interpretation:
When more polar solvent is used, the affect on rate of given SN2 reaction is to be given.
Concept Introduction:
The SN2/E2 reaction of
An SN2 reaction of an alkyl halide is favoured by a high concentration of a good (neutral)
in a protic polar solvent.
(b)
Interpretation:
When more polar solvent is used, the affect on rate of given SN2 reaction is to be given.
Concept Introduction:
The SN2/E2 reaction of alkyl halide is with neutral nucleophile/base, the increasing polarity of the solvent will increase the rate of the reaction is to be identified.
An SN2 reaction of an alkyl halide is favoured by a high concentration of a good (neutral)
in a protic polar solvent.
(c)
Interpretation:
When more polar solvent is used, the affect on rate of given SN2 reaction is to be given.
Concept Introduction:
The SN2/E2 reaction of alkyl halide is with neutral nucleophile/base, the increasing polarity of the solvent will increase the rate of the reaction is to be identified.
An SN2 reaction of an alkyl halide is favoured by a high concentration of a good (neutral)
in a protic polar solvent.
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Organic Chemistry (8th Edition)
- There is great excess of H2O in this reaction.arrow_forward5. w mexico What is the likely mechanism of this reaction? ew mexico Br A. E1cb B. E1 C. E2 D. None of the choices are correct. NaNH, DMF 6. I can answer question #5 because I know that: A. The solvent is polar protic, so a cation is easily formed B. The base is ionic, and so is a strong base C. The product follows Zaitsev's Rule D. The stability of the conjugate base allows for easy deprotonation as a first steparrow_forwardNH3(g) + HCIO4(1) E→ NH,CI0,(s) A B C D Ep E, Ep - R P R P R R Reaction Path Reaction Path Reaction Path Reaction Path Aarrow_forward
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