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- Which of the following compounds (A or B) would experience a faster SN1 reaction?Is this an E1, E2, SN1, or SN2 and is it elimination or substitution.Arrange the following alkyl halides in increasing reactivity in E2 reaction. Write 1 for the least reactive, then 2 and 3 for the most reactive Answer: A. _____ B. _____ C. _____
- Rank A, B, and C in order of increasing SN1 reactivity.Provide the complete mechanism using Curved Arrow Formalism for the reaction of 1-chloro-1-methylcyclopentane treated with NaOMe in MeOH. If more than one product is formed, which is the major, minor, and very minor product? Is the reaction SN1, SN2, E1, or E2. I appreciate the help on this question.Which of the following are achiral? And identify the relationship between each of them. Ex. A-B, B-D
- what mechanism is involved? SN1, E2, E1, or SN2Draw a detailed mechanism for the FeBr3@catalyzed reaction of ethylbenzene with bromine, and show why the sigma complex (and the transition state leading to it) is lower in energy for substitution at the ortho and para positions than it is for substitution at the meta position.How does each of the following changes affect the rate of an E2 reaction? (a, b, and c)
- Which of the products will react the fastest given an SN2 reaction ?Of the two molecules below select which molecule would be predicted to react faster via an E2 elimination. (hint: stereoelectronic arguments can help)Arrange the following according to INCREASING reactivity towards E2: 1st ( least reactive)? 2nd? 3rd? 4th (most reactive)?