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Assertion: Phenols give o- and p-nitrophenol on nitration with conc. \[\ce{HNO3}\] and \[\ce{H2SO4}\] mixture.
Reason: –OH group in phenol is o–, p– directing.
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Write complete reaction for the bromination of phenol in aqueous and non-aqueous medium.
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Explain why Lewis acid is not required in bromination of phenol?
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How can phenol be converted to aspirin?
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In Clemmensen Reduction carbonyl compound is treated with:
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Treatment of compound \[\begin{array}{cc}
\phantom{.....}\ce{O}\\
\phantom{.....}||\\
\ce{Ph - O - C - Ph}
\end{array}\] with \[\ce{NaOH}\] solution yields
(i) Phenol
(ii) Sodium phenoxide
(iii) Sodium benzoate
(iv) Benzophenone
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Arrange the following in decreasing order of their acidic strength. Give explanation for the arrangement.
\[\ce{C6H5COOH, FCH2COOH, NO2CH2COOH}\]
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Assertion: Compounds containing \[\ce{-CHO}\] group are easily oxidised to corresponding carboxylic acids.
Reason: Carboxylic acids can be reduced to alcohols by treatment with \[\ce{LiAlH4}\].
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Write down functional isomers of a carbonyl compound with molecular formula \[\ce{C3H6O}\]. Which isomer will react faster with \[\ce{HCN}\] and why? Explain the mechanism of the reaction also. Will the reaction lead to the completion with the conversion of whole reactant into product at reaction conditions? If a strong acid is added to the reaction mixture what will be the effect on concentration of the product and why?
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The letters ‘D’ or ‘L’ before the name of a stereoisomer of a compound indicate the correlation of configuration of that particular stereoisomer. This refers to their relation with one of the isomers of glyceraldehyde. Predict whether the following compound has ‘D’ or ‘L’ configuration.

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Assertion: All naturally occurring α-aminoacids except glycine are optically active.
Reason: Most naturally occurring amino acids have L-configuration.
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A natural linear polymer of 2-methyl-1, 3-butadiene becomes hard on treatment with sulphur between 373 to 415 K and – S – S – bonds are formed between chains. Write the structure of the product of this treatment?
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Identify the type of polymer given in the following figure.

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To have practical applications why are cross links required in rubber?
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Why does cis-polyisoprene possess elastic property?
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What is the structural difference between HDP and LDP? How does the structure account for different behaviour and nature, hence the use of a polymer?
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Assertion: Network polymers are thermosetting.
Reason: Network polymers have high molecular mass.
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Which is the correct statement about birth control pills?
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The most useful classification of drugs for medicinal chemists is ______.
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