Important Questions of Organic Chemistry – Some Basic Principles and Techniques Chemistry | Zigya

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321.

In a mixture, two enantiomers are found to be present in 85% and 15% respectively. The enantiomeric excess (ee) is

  • 85%

  • 15%

  • 70%

  • 60%


322.

Among the following structures the one which is not a resonating structure of others is

            

  • I

  • II

  • III

  • IV


323.

In the Lassaigne's test for the detection of nitrogen in an organic compound, the appearance of blue coloured compound is due to

  • ferric ferricyanide

  • ferrous ferricyanide

  • ferric ferrocyanide

  • ferrous ferrocyanide


324.

The IUPAC name of the compound X is

  • 4-cyano-4-methyl-2-oxopentane

  • 2-cyano-2-methyl- 4-oxopentane

  • 2, 2-dimethyl-4-oxopentanenitrile

  • 4-cyano-4-methyl-2-pentanone


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325.

(+)-2-chloro-2-phenylethane in toluene racemises slowly in the presence of small amount of SbCl2, due to the formation of

  • carbanion

  • carbene

  • free-radical

  • carbocation


326.

Correct pair of compounds which gives blue colouration/precipitate and white precipitate, respectively, when their Lassaigne's test is separately done is

  • NH2NH2, HCl and ClCH2COOH

  • NH2CSNH2 and PhCH2Cl

  • NH2NH2, COOH and NH2CONH2


327.

2-methylpropane on monochlorination under photochemical condition give

  • 2-chloro-2-methylpropane as major product

  • (1 : 1) mixture of 1-chloro-2-methylpropane and 2-chloro-2-methyl propane

  • 1-chloro-2-methyl propane as a major product

  • (1 : 9) mixture of 1-chloro-2-methylpropane and 2-chloro-2-methylpropane


328.

The most likely protonation site in the following molecule is    

                        

 

  • C-1

  • C-2

  • C-3

  • C-6


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329.

The optically active molecule is


330.

An optically active compound having molecular formula C2H16 on ozonolysis gives acetone as one of the products. The structure of the compound is


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