UNIT 7: Alcohols, Phenols and Ethers

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Dehydration of alcohol is an example of:

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Phenoxide ion stability is due to:

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Boiling point order:

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Phenol does not undergo:

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Alcohol + carboxylic acid gives:

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Ether is soluble in water due to:

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Williamson synthesis follows:

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Electron withdrawing group increases:

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Weakest acid:

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Strongest acid:

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Ether formation from alcohol uses:

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Phenol reacts with bromine water to form:

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Ethers are:

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Phenol is less acidic than:

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Anisole is:

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Ether cleavage occurs with:

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Reimer-Tiemann reaction gives:

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Kolbe reaction produces:

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Phenol nitration gives:

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Phenol gives violet color with:

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Tertiary alcohol on oxidation gives:

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Secondary alcohol oxidation gives:

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Oxidation of primary alcohol gives:

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Alcohol dehydration gives:

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Phenol reacts with NaOH to form:

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Tertiary alcohol reacts fastest in Lucas test because:

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Lucas test distinguishes:

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Reaction of alcohol with Na gives:

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Phenol is more acidic than alcohol due to:

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Boiling point of alcohols is high due to:

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Methanol is industrially prepared from:

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Phenol is prepared from benzene sulphonic acid by:

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Hydrolysis of alkyl halides gives:

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Ether formation involves reaction of:

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Williamson synthesis is used to prepare:

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Cumene process gives:

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Phenol is prepared from chlorobenzene by:

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Reduction of ketone gives:

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Grignard reagent reacts with aldehydes to give:

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Alcohols can be prepared by hydration of:

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Ether is polar due to:

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Alcohols show hydrogen bonding due to:

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Phenol is:

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Tertiary alcohol example:

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Which is secondary alcohol?

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Which is a primary alcohol?

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General formula of alcohols is:

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Ether linkage is:

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Phenols differ from alcohols because –OH is attached to:

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The functional group of alcohols is:

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