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What is the product of E2 elimination or (3R,4R)-3-chloro-2,2,4-trimethylhexane?
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- What is the major E2 elimination product formed from attached halide?The Hofmann product is favored by the E2 mechanism when 2-bromo-3-methylbutane is added: A. MeOH B. MeO:- in MeOH C. Nal in acetona D. (CH 3)3 CO:- in (CH 3),COHExplain why α-pyrone reacts with Br2 to yield a substitution product (likebenzene does), rather than an addition product to one of its C=C bonds.
- Iodoethane does not react via Sn2 reaction with NaI in Acetone. It is a good leaving group and on the primary carbon, why doesn't it react Sn2? (I know it reacts Sn1)1-Bromobutane would react with HS- via _______ reactiona.) SN1 b.) SN2 c.) E1 d.) E2Show the relationship between E2 Reactions and Alkyne Synthesis ?
- Increasing the number of R groups on the carbon with the leaving group forms more highly substituted, more stable alkenes in E2 reactions. Explain this ?SN1 is always a competing reaction of E1. True or False?How many distinct alkene products are possible when the alkyl iodide below undergoes E2 elimination?