Which of the following statements are correct? Mark all that apply. Select 4 correct answer(s) Strength of nucleophile does not affect the rate of the SN1 reactions Good leaving group speeds up both SN2 reaction and SN1 reaction Hydroxide ion is not a good leaving group, but it can be activated by protonation Formation of carbocation is the slow step of reaction in SN1

Draw the major product of this SN1 reaction. Ignore any inorganic byproducts.

lost on this guy as well Be sure to answer all parts. Determine a stepwise mechanism for the following reaction that illustrates why two substitution products are formed. Explain why 1-bromohex-2-ene reacts rapidly with a wide ph Meme under Sx1 reaction conditions, even though it is a 1° alkyl halide. 1-bromohex-2-ene CH₂OH Part 1: The first step in the reaction proceeds according to which mechanism? CH₂CH₂CH₂CH=CHCH₂ CH₂CH₂CH₂CH=CHCH₂ + CH₂OH Part 2 out of 5 Draw the missing resonance contributor. Check my work OCH₁ CH₂CH₂CH₂CH=CH-CH₂ + Br CH₂CH₂CH₂CH=CHCH₂ CH OCH₂ edit structure... Next part +HBr

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