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An organic compound XC5H10 on ozonolysis gives Y&Z. The product mixture Y and Z on reaction with NH2OH gives four oximes. The structure of X is:

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Important Questions on Practical Organic Chemistry

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Compound AC8H12 does not show stereoisomerism. It adds only one mole of H2. On ozonolysis, it gives a symmetrical diketone BC8H12O2. Identify A.
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Compound 'A' C3H6O, decolourises Br2 water. It liberates colourless, odourless gas on addition of sodium metal. On ozonolysis, it gives B and compound  'C'C2H4O2, Identify 'A'.
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A compound PC5H6 gives Baeyer's test positive and on hydrogenation form a hydrocarbon BC5H10, B gives only one monochloro product. The compound P is:
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Compound 'A' C16H18 on ozonolysis gives only one product 'B',C8H8O. 'B' gives positive iodoform test and forms sodium benzoate as one of the products. Identify the structure of 'A'.
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Compound XC3H6O gives negative tests with the following reagents. (a) Br2 (b) 2, 4-Dinitrophenylhydrazine (c) Na metal. It gives two monochloro structural isomers. Identify 'X'.
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The following two compounds I and II can be distinguished by using reagent

Question Image

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An organic compound with molecular formula C6H8, on reductive ozonolysis gives 2 moles of 2 -oxopropanal. The structure of the compound will be
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The incorrect statement about Question Image is: