Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: HBr Br ОН OH Part 1 out of 3 HO HOBR H2O Br draw structure finish structure HBr Next part of 11 Prev FI F11 F10 F8 F9 F6 F7 F5 F4
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- Draw a stepwise mechanism for the following reaction that illustrates how two substitution products are formed. Explain why 1-bromohex-2ene reacts rapidly with a weak nucleophile (CH3OH) under SN1 reaction conditions, even though it is a 1 ° alkyl halide.(a) Which compound in each of the following pairs will react faster in SN2 reaction with -OH group?(i) CH3Br or CH3I(ii) (CH3)3CCl or CH3ClWrite a stepwise mechanism for the following reactions. Please answer correct i will give you upvote but answer all correct
- This is Wittig Rxn: Whatever mechanism you choose to draw is fine since you can leave the base as B: Draw the arrow pushing mechanism using the compounds below – Constant: 4-nitrobenzyl benzaldehydebase 1: triethylaminebase 2: NaOHbase 3: K2CO3ylide: Acetonyltriphenylphosphonium chlorideDraw a stepwise mechanism for the following reaction that illustrates how two substitution products are formed. Explain why 1-bromohex-2-ene reacts rapidly with a weak nucleophile (CH3OH) under SN1 reaction conditions, even though it is a 1° alkyl halide.4-Methylpyridine reacts with benzaldehyde (C6H5CHO) in the presence of base to form A. (a) Draw a stepwise mechanism for this reaction. (b) Would you expect 2- methylpyridine or 3-methylpyridine to undergo a similar type of condensation reaction? Explain why or why not.
- Provide the suitable reagents to effect the following transformations. I specifically need help on sub-parts d, e, f, g, h, and i.4-Methylpyridine reacts with benzaldehyde (C6H5CHO) in the presence of base to form A. (a) Draw a stepwise mechanism for this reaction. (b) Would you expect 2-methylpyridine or 3-methylpyridine to undergo a similar type ofcondensation reaction? Explain why or why not.Draw a stepwise mechanism for the attached reaction that illustrateshow two substitution products are formed. Explain why 1-bromohex-2-ene reacts rapidly with a weak nucleophile (CH3OH) under SN1 reactionconditions, even though it is a 1 ° alkyl halide.
- When allyl bromide is refluxed with magnesium metal in ether solvent, the product formed is 1,5-hexadiene. (C6H10). What is the curved arrow mechanism for this reaction?Answer the following questions based on the compounds below: (pictures) a) Which compound has the lower boiling point? Explain. b) Draw the SN1 mechanism for the reaction of compound B with sodiumhydroxide, NaOH.Fill in the missing reagents below.