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How is propanoic acid is prepared to start from alcohol?
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How is propanoic acid is prepared to start from an alkyl halide?
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How is propanoic acid is prepared to start from an alkene?
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An alkene (A) on ozonolysis gives propanone and aldehyde (B). When (B) is oxidised (C) is obtained. (C) is treated with Br2/P gives (D) which on hydrolysis gives (E). When propanone is treated with HCN followed by hydrolysis gives (E). Identify A, B, C, D and E.
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Oxidation of ketones involves carbon-carbon bond cleavage. Name the product(s) is/are formed on oxidising 2, 5-dimethyl hexan-3-one using a strong oxidising agent.
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Which of the following reagent can be used to convert nitrobenzene to aniline?
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The method by which aniline cannot be prepared is ____________.
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Which one of the following will not undergo Hofmann bromamide reaction?
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\[\ce{CH3CH2Br ->[aq NaOH][\Delta] A ->[KMnO4/H^+][\Delta] B ->[NH3][\Delta] C ->[Br2/NaOH] D}\] ‘D’ is:
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Which one of the following nitro compounds does not react with nitrous acid?
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Which of the following reaction is not correct.
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Nitrobenzene on reaction with at 80-100°C forms which one of the following products?
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C5H13N reacts with HNO2 to give an optically active compound – The compound is ____________.
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Secondary nitro alkanes react with nitrous acid to form ____________.
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When
is reduced with Sn/HCl the pair of compounds formed are ____________.
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Among the following, the reaction that proceeds through an electrophilic substitution is:
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Write down the possible isomers of the C4H9NO2 give their IUPAC names.
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There are two isomers with the formula CH3NO2. How will you distinguish between them?
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What happens when 2-Nitropropane boiled with HCl?
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