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Q: Reaction of 5,5-dimethoxypentan-2-one with methylmagnesium iodide followed by treatment with aqueous…
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Q: (d) Draw the E1 mechanism for the reaction of 2-chloro-2-methylbutane with sodium hydroxide, NaOH.
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A: Applying concept of substitution and elimination reaction.
Q: Reaction of 5,5-dimethoxypentan-2-one with methylmagnesium iodidefollowed by treatment with aqueous…
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- Epoxides are converted to allylic alcohols with nonnucleophilic bases such as lithium diethylamide [LiN(CH2CH3)2]. Draw a stepwise mechanism for the conversion of 1,2-epoxycyclohexane to cyclohex-2en-1-ol with this base. Explain why a strong bulky base must be used in this reaction.Epoxides are converted to allylic alcohols with nonnucleophilic basessuch as lithium diethylamide [LiN(CH2CH3)2]. Draw a stepwisemechanism for the conversion of 1,2-epoxycyclohexane to cyclohex-2-en-1-ol with this base. Explain why a strong bulky base must be used inthis reaction.What is the detailed reaction mechanism between 1-indanone and veratraldhyde, with a NaOH base and no solvant? The final product should be 2-(3,4-dimethoxybenzylidene)-1-indanone. Please include arrows and charges. Thank you.
- 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.Draw a stepwise mechanism for the conversion of hex-5-en-1-ol to the cyclic ether A.Draw the products formed when p-methylaniline (p-CH3C6H4NH2) is treated with each reagent.a. HClb. CH3COClc. (CH3CO)2Od. excess CH3Ie. (CH3)2C = Of. CH3COCl, AlCl3g. CH3CO2Hh. NaNO2, HCli. Part (b), then CH3COCl, AlCl3j. CH3CHO, NaBH3CN
- 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.2-Methylpropane have more than one kind of hydrogen and will generate 2 different products with bromination in the presence of uv light. t or fDraw the products formed when p-methylaniline (p-CH3C6H4NH2) istreated with following reagent. Part (b), then CH3COCl, AlCl3
- Draw the Robinson annulation product(s) formed by reaction of 2-acetylcyclopentanone with methyl vinyl ketone (CH2=CHCOCH3).Draw 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.Show a stepwise mechanism by pushing arrows and drawing all intermediates. Draw a detailed mechanism for the addition of H2O to 2-methyl-2-pentene in the presence of H2SO4.
