2- Mention the product of a nucleophilic substitution reaction of (S)-2- bromohexane with acetate ion, CH3CO2- Assume that inversion of configuration occurs, and show the chemistry of both the reactant and product.
2- Mention the product of a nucleophilic substitution reaction of (S)-2-
bromohexane with acetate ion, CH3CO2-
Assume that inversion of configuration occurs, and show the chemistry
of both the reactant and product.
3- Draw the mechanism of the SN2 Reaction. Show the correct directions
of the arrows, and all reagents.
4- Draw the mechanism of the SN1 Reaction. Show the correct directions
of the arrows, and all reagents.
5- Draw the mechanism of the E2 Reaction with an
the correct directions of the arrows, and all reagents.
6- Draw the mechanism of the E1 Reaction with an Alkyl Halide. Show
the correct directions of the arrows, and all reagents.
7- Mention the product formed in an SN2 reaction between 1-
bromobutane and NaI.
8- Rank the following compounds in order of their expected reactivity
toward SN2 reaction: CH3Br, CH3OTos, (CH3)2CHCl.
9- Explain Grignard Reagents in details with one example.
10- Mention how a halogen substituent can be replaced by a
deuterium atom in the preparation of a deuterated compound.
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