The correct structure of C is
The Correct Option is A
Solution and Explanation
Top Questions on Alcohols, Phenols and Ethers
- An alcohol X (C$_4$H$_{10}$O) reacts with Conc.HCl/ZnCl$_2$ to give corresponding chloride. X on dehydration forms Y, which reacts with Baeyer's reagent to give Z. What is Z?
- TS EAMCET - 2025
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Given below are two statements:
Statement I: Dimethyl ether is completely soluble in water. However, diethyl ether is soluble in water to a very small extent.
Statement II: Sodium metal can be used to dry diethyl ether and not ethyl alcohol.
In the light of the given statements, choose the correct answer from the options given below:- JEE Main - 2025
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- Isopentyl alcohol reacts with reagent X → carboxylic acid → decarboxylation → Y. Reaction of Y with Z → t-butyl alcohol. Identify X and Z.
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- In which of the following, intramolecular hydrogen bonding is present?
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- Distinguish between Alcohol and Phenol.
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Questions Asked in JEE Main exam
- The value of \( (\sin 70^\circ)(\cot 10^\circ \cot 70^\circ - 1) \) is:
- JEE Main - 2025
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- Find the equivalent resistance between two ends of the following circuit:
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- Current electricity
If A and B are two events such that \( P(A \cap B) = 0.1 \), and \( P(A|B) \) and \( P(B|A) \) are the roots of the equation \( 12x^2 - 7x + 1 = 0 \), then the value of \(\frac{P(A \cup B)}{P(A \cap B)}\)
- JEE Main - 2025
- Probability
- The sum of all local minimum values of the function \( f(x) \) as defined below is:
\[ f(x) = \begin{cases} 1 - 2x & \text{if } x < -1, \\[10pt] \frac{1}{3}(7 + 2|x|) & \text{if } -1 \leq x \leq 2, \\[10pt] \frac{11}{18}(x-4)(x-5) & \text{if } x > 2. \end{cases} \]- JEE Main - 2025
- Functions
- Number of functions \( f: \{1, 2, \dots, 100\} \to \{0, 1\} \), that assign 1 to exactly one of the positive integers less than or equal to 98, is equal to:
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Concepts Used:
Preparation - Alcohols, Phenols and Ethers
Alcohols, phenols, and ethers are organic compounds that can be prepared by various methods.
Preparation of Alcohols:
- Direct hydration of alkenes: Alcohols can be prepared by the addition of water to an alkene in the presence of a strong acid catalyst.
- Reduction of carbonyl compounds: Alcohols can be prepared by the reduction of aldehydes, ketones, or carboxylic acids using reducing agents like NaBH4 or LiAlH4.
- Grignard reaction: Alcohols can be prepared by reacting Grignard reagents with carbonyl compounds.
- Hydroboration-oxidation: Alcohols can be prepared by the hydroboration of alkenes followed by oxidation with an oxidizing agent like H2O2.
Preparation of Phenols:
- Hydrolysis of diazonium salts: Phenols can be prepared by the hydrolysis of diazonium salts, which are formed by the reaction of aniline with nitrous acid.
- Oxidation of sulfonic acids: Phenols can be prepared by the oxidation of sulfonic acids using strong oxidizing agents like potassium permanganate or chromic acid.
Preparation of Ethers:
- Williamson synthesis: Ethers can be prepared by the reaction of an alkoxide ion with a primary alkyl halide or tosylate in the presence of a strong base like NaOH or KOH.
- Dehydration of alcohols: Ethers can be prepared by the dehydration of alcohols in the presence of a strong acid catalyst like H2SO4.
In summary, alcohols, phenols, and ethers can be prepared by a variety of methods, including hydration, reduction, Grignard reaction, hydroboration-oxidation, hydrolysis, oxidation, Williamson synthesis, and dehydration. The choice of the method depends on the availability of starting materials, the desired product, and the conditions of the reaction.