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Aldehydes and ketones react with hydroxylamine to form ______.
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The slope in the plot of `log ["R"]_0/(["R"])` Vs. time for a first-order reaction is ______.
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When D-glucose reacts with HI, it forms ______.
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Solubility of gas in liquid decreases with increase in ______.
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Which of the following molecules has a chiral centre correctly labelled with an asterisk (*)?
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Assertion (A): Trans [CrCl2(ox)2]3− shows optical isomerism.
Reason (R): Optical isomerism is common in octahedral complexes involving didentate ligands.
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Give the reaction of glucose with hydrogen cyanide. Presence of which group is confirmed by this reaction?
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Give a reason for the following observations:
Penta-acetate of glucose does not react with hydroxylamine.
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In which of the following solvents, the \[\ce{C4H8NH3+X–}\] is soluble?
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Radioactive decay follows first-order kinetics. The initial amount of two radioactive elements X and Y is 1 gm each. What will be the ratio of X and Y after two days if their half-lives are 12 hours and 16 hours respectively?
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Out of p-tolualdehyde and p-nitrobenzaldehyde, which one is more reactive towards nucleophilic addition reactions, why?
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Write the structure of the product formed when acetone reacts with 2, 4 DNP reagent.
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Arrange the decreasing boiling point.
\[\ce{CH3COOH, C2H5OH, CH3NH2, CH3OCH3}\]
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Write the two applications of Henry’s law.
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Amongst the following compounds, identify which are insoluble, partially soluble and highly soluble in water?
- phenol
- toluene
- formic acid
- ethylene glycol
- chloroform
- pentanol
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Give an example of the reaction in the following case.
Oxime
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Give an example of the reaction in the following case.
Imine
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Sucrose decomposes in acid solution to give glucose and fructose according to the first order rate law. The half life of the reaction is 3 hours. Calculate fraction of sucrose which will remain after 8 hours.
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Arrange the following in increasing order of their basic strength in aqueous solution:
\[\ce{CH3NH2, (CH3)3N, (CH3)2NH}\]
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For a first order reaction, show that time required for 99% completion is twice the time required for the completion of 90% of reaction.
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