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- Rank the nucleophiles in each group in order of increasing nucleophilicity.a. -OH, -NH2, H2Ob. -OH, Br-, F- (polar aprotic solvent)c. H2O, -OH, CH3CO2-Which halide in the attached marine natural product reacts fastest inthe SN2 reaction?Write the products for (A-I). Label products with the mechanism (Sn2, Sn1, E1, E2) that produced it and write out and label major vs minor elimination products.
- Rank the following compounds (an SN2 reaction with NaCN) with 1(the fastest reaction) and 4(slowest.)Please explain the steps of this synthesis. Identify SN1, SN2, E2 or E1. Identify the nucleophile and electrophilesWhich compound would undergo carbocation rearrangement during an SN1 reaction? A B C D
- Draw the major product and state wheter the reaction is SN2, E2, SN1, or E1Rank these alkyl halides in order of increasing reactivity in an SN2 reaction1. Draw a reasonable arrow-pushing mechanism for the transformation shown along. 2. Identify nucleophiles and electrophiles 3. Name any type of reactions taking place like E2 or E1 4. Account for any regio- or stereoselectivity