(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
- Q1: Draw a valid Lewis structures for the following molecules. Include appropriate charges and lone pair electrons. If there is more than one Lewis structure available, draw the best structure. NH3 Sulfate Boron tetrahydride. C3H8 (linear isomer) OCN NO3 CH3CN SO2Cl2 CH3OH2*arrow_forwardIn the following molecule, indicate the hybridization and shape of the indicated atoms. -z: CH3 CH3 H3C HO: CI: :arrow_forwardQ3: Draw the Lewis structures for nitromethane (CH3NO2) and methyl nitrite (CH3ONO). Draw at least two resonance forms for each. Determine which form for each is the major resonance contributor. Page 1 of 4 Chem 0310 Organic Chemistry 1 Recitations Q4: Draw the Lewis structures for the cyanate ion (OCN) and the fulminate ion (CNO-). Draw all possible resonance structures for each. Determine which form for each is the major resonance contributor.arrow_forward