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Identify A, B, C, D and write the complete equation.
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What will be the product (X and A) for the following reaction?
\[\ce{acetylchloride ->[i) CH3MgBr][ii) H3O^+] X ->[acid K2Cr2O7] A}\]
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How will you convert acetylene into n-butyl alcohol?
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3, 3-dimethyl butane-2-ol on treatment with conc. H2SO4 to give tetramethyl ethylene as a major product. Suggest a suitable mechanism.
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The IUPAC name of

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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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