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- What is the structure of the major organic product that would result from acid-catalyzed dehydration of 3,3-dimethyl-2-butanol whose structure is listed.Provide reactants/reagents and solvents that could be used to synthesize these products from an alkyl halide via substitution or elimination.Provide the structure of the carbene that results when diazomethane decomposes.
- Identify by describing the structure of the products that will form when acid-catalyzed water is removed from trans-2-methyl cyclohexanol and sodium methoxide base and hydrogen bromide are removed from trans-1-bromo 4-methyl cyclohexane.Explain why the acid-catalyzed dehydration of an alcohol is a reversible reaction, whereas the base-promoted dehydrohalogenation of an alkyl halide is an irreversible reaction.Draw the structure of the major product that would be obtained from the dehydration of 3,5-dimethylcyclohexanol and explain
- illustrate the chemical equation of N,N- Dimethyl aniline reacts with Diazotized Sulfanilic acid to form Methyl OrangeWrite the reagents used to synthesise the following compound starting from the benzoic acidWrite the overall chemical equation and the steps involved in the synthesis of isoheptane by the acid catalysed alkylation reaction.
- What change can be made to allow for a faster rate of reaction if poor solubility of KOH in ethanol slowed the rate and led to slow deprotonation of dibenzyl ketone?Draw the structural formula of the enol formed in the following alkyne hydration reaction and then draw the structural formula of the carbonyl compound with which this enol is in equilibrium.Predict the alcohols that would give this oxidation product: