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- Which alcohols can be prepared as a single product by hydroboration–oxidation of an alkene? Which alcohols can be prepared as a singleproduct by the acid-catalyzed addition of H2O to an alkene?Draw a structural formula for the product of the acid-catalyzed hydration of 1-methylcyclohexene.Consider the reaction between an alcohol and tosyl chloride, followed by a nucleophile. Write the condensed formula of the expected main organic product. CH3OH −→−−−−−−−−2. CH3S−1. TsCl,pyridine
- 1.Give the common name of 2,2-dimethyl-1-propanethiol and give the complete equation as the compound is exposed to oxidation. 2.What will be the product of the compound in #1 if added with NaOH?What is the biological reducing agent that gives rise to the formation of chiral ethyl 3-hydroxybutanoate?Give the products, if any, of the benzoic acid + CH3CH2Cl + AlCl3 reaction:
- What is the product of the reduction of 3-methyl-2-butanone? Include a structure of the product.Which alcohols can be prepared as a single product by hydroboration– oxidation of an alkene? Which alcohols can be prepared as a single product by the acid-catalyzed addition of H2O to an alkene?Write structural formulas for the products formed in each of the following reactions, and categorize the type of reaction involved (a) CH3CH2CHO + (O) → (b) CH3CH=CH2 + HBr →
- Name the major product of the reaction between (S)-2-bromohexane and KCH3COO.Draw the principal organic reactants, reagents, or products of the following reactions. Fill out the blank, for products, draw all major products showing stereo isomers, if present.Write the structural formula for the product of each reaction.