Q. The catalyst which is used to break hydrocarbons is

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Q. Aluminum oxide does not react with

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Q. Aluminum oxide reacts as an acid upon reaction with

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Q. Aluminum oxide (Al₂O₆) reacts as a base (OH⁻) upon reaction with

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Q. Hydrolysis of substituted amides will give the product of

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Q. By refluxing unsubstituted amide with acid, it will yield

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Q. Ethanoyl chloride will react with concentrated ammonia solution to produce

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Q. CH₃CONH₂ is formula for

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Q. Structural formula -CONH₂ is representing

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Q. Amides give products of sodium salt of carboxylic acid and primary amine in presence on aqueous sodium hydroxide by reacting with

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Q. Amides are refluxed for hydrolysis by

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Q. Two hydrocarbon section of amide molecules are linked together by group

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Q. Amines which are bonded in Alkyl group are

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Q. Trim ethylamine is an example of

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Q. Phenyl amine is involved importantly in the synthesis of

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Q. One of three p-orbitals on nitrogen atom overlaps with pi bonding system in 'benzene ring' in the molecule of

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Q. In the production of phenylamine, it is separated from the reaction mixture by process of

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Q. Comparing the pH level of ethylamine and ammonia, the stronger base is

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Q. Amines and its derivatives are used to treat diseases like

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Q. The reaction between phenylamine and nitrous acid produce diazonium ion while making azo dye is called

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