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A: a.
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Identify all possible product(s) in the following reactions.
a) 1-bromocyclohexane with sodium hydroxide.
b) 2-chloro-2-methylpentane with water
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- Draw the structure of each product from the reaction of benzene with 2-chloro-1-methylcyclohexane using AlCl 3 as the catalyst and Identify the major product.How many products including stereoisomers are formed when 2,4-dimethylpentane undergoes monochlorination?If 1-bromopentane is heated in acetone containing NaOH, what is the alkane produced? Draw and explain the step-by-step mechanism of the production of the compound
- Consider the structure of cyclohexyne, if it undergoes acetylide reaction with NaNH2 and 2 moles of CH3Br, which of the following final product is formed? a. 1,2-methylcyclohexyne HBr b. 1-methylcyclohexyne c. No reactionAn unknown alcohol with a molecular formula of C7H14O was oxidized to an aldehyde with HOCl. When an acidic solution of the alcohol was distilled, two alkenes were obtained. The alkene formed in greater yield was determined to be 1-methylcyclohexene. The other alkene formed the original unknown alcohol when treated with BH3/THF followed by H2O2, HO-, and H2O. Identify the unknown alcohol.An unknown alcohol with a molecular formula of C7H14O was oxidized to an aldehyde with HOCl. When an acidic solution of the alcohol was distilled,two alkenes were obtained. The alkene formed in greater yield was determined to be 1-methylcyclohexene. The other alkene formed the original unknown alcohol when treated with BH3/THF followed by H2O2, HO-, and H2O. Identify the unknown alcohol.
- Draw the structure of two alkenes that would yield 1‑methylcyclohexanol when treated with Hg(OAc)2Hg(OAc)2 in water, then NaBH4NaBH4Identify two alkenes that react with HBr to form 1-bromo-1-methylcyclohexane without undergoing a carbocation rearrangement.Draw the structure of an eight‑carbon alkene that would yield the following compound (and no others) after treatment with ozone followed by dimethyl sulfide. draw the starting alkene
- Identify the reaction of the following reaction: a. formation of (R)-1-methoxypentane from (S)-1-bromopentane b. production of trans- and cis-2-butene from 2-chlorobutane c. Conversion of trans-1-chloro-2-methylcyclopentane to 1-methylcyclopentene d. formation of (S)-2-butanol from (S)-2-bromobutaneWhich one(s) of the following reactions produce propan-1-ol? A) the alkaline hydrolysis of 1-chloropropane B) the acid hydrolysis of propyl methanoate C) the acid hydrolysis of propanenitrilewhat are the reagents/conditions that would transform cyclohexanol to 1-methylcyclohexene.?