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A

Alcohol Oxidation with Potassium Dichromate

Potassium dichromate oxidises 1o and 2o alcohols and gets reduced to green Cr3+ ion.

In case of 3o alcohols the bright orange colour of dichromate ion remains as it is indicating no reaction.

The colour change can be used to indicate a reaction. If the orange colour changes to green or blue green a reaction has occurred.

fig.

Alkyl Halide Nucleophilic Substitution/Elimination

Primary: Generally SN2 is better than E2. E2 is favoured by strong bulky base with heating as bulky base finds is harder to reach C than H due to steric hindrance

Secondary: SN2 is favoured over E2 if nucleophile is weak base and the solvent is polar and aprotic. E2 is favoured over SN2 if strong base is used in protic solvent. Heating further favours E2 over SN2. Reactions can go via SN1 and E1 mechanisms in protic solvents.

Tertiary: E2 is almost exclusive in the presence of strong base and protic solvent.