Chemistry Chapter 13 Entry Test MCQs

colesterol structure

a. zero
b. Two
c. Eight
d. one

c. Eight

a. Geometric isomers
b. Optically Active compounds
c. Structural isomers
d. Meso Compounds

b. Optically Active compounds

a. Molecular formula
b. Structural formula
c. Physical properties
d. Chemical properties

a. Molecular formula

a. 3
b. 1
c. 4
d. 2

d. 2

a. 4
b. 2
c. 6
d. 3

c. 6

a. Two groups linked to carbon atom are different
b. Four groups linked to carbon atom are different
c. All the groups linked to carbon atom are same
d. Three groups linked to carbon atom are different

b. Four groups linked to carbon atom are different

a. 4
b. 6
c. 8
d. 9

a. 4

a. Isomers that only differ by rotations around single bonds.
b. Stereisomers that are nonsuperimposable non mirror images.
c. Isomers that only differ in the bonding arrangement of the atoms.
d. Stereisomers that are nonsuperimposible mirror images.

b. Stereisomers that are nonsuperimposable non mirror images.

a. 2-hexyne
b. 2-butene
c. Lactic acid
d. 2,2-dimethylpropane

c. Lactic acid

a. Butanone and butanal
b. Ethyl ethanoate and methyl propanoate
c. Methoxy methane and ethanol
d. Ethoxy propane and propoxy methane

d. Ethoxy propane and propoxy methane

a. Carbon atom of the methyl group
b. Central carbon atom
c. Oxygen of the hydroxyl groups
d. Carbon atom of the carboxylic acid group

b. Central carbon atom

a. CH2 = CH – CH(OH) – CH3
b. CH3 – CH2 – CH2 – CHO
c. (CH3) 2 CH – CHO
d. CH2 – CO – CH2 – CH3

a. CH2 = CH – CH(OH) – CH3

a. 7
b. 5
c. 8
d. 6

d. 6

a. Propane
b. Pentane
c. Propene
d. Ethanol

a. Propane

a. 4
b. 2
c. 5
d. 3

a. 4

a. CH3CH2OCH = CHCH2CH3
b. CH3CH = CHCH2CH2CHO
c. (CH3)2CH – CO – CH2CH3
d. CH3CH2COCH2CH2CH3

b. CH3CH = CHCH2CH2CHO

a. CH3 – CO – C2H5
b. CH3 – O – C2H5
c. C2H5 – S – C2H5
d. CH3 – O – CH3

c. C2H5 – S – C2H5

a. Functional group isomers
b. Cis-trans isomers
c. Chain isomers
d. Metamers

a. Functional group isomers

a. Dipole moment
b. Melting point
c. Boiling point
d. All of these

d. All of these

a. Prototropism
b. Chain isomerism
c. Geometrical isomerism
d. Metamerism

a. Prototropism

a. Trans-2-butene
b. 2-methyl-1-propene
c. Cis-2-butene
d. 1-butene

a. Trans-2-butene

a. 4
b. 2
c. 6
d. 3

c. 6

a. 4
b. 3
c. 10
d. 7

d. 7

a. Glycerol
b. Ethylene glycol
c. Tartaric acid
d. Oxalic acid

c. Tartaric acid

a. 5
b. 3
c. 6
d. 4

d. 4

a. 3
b. 1
c. 4
d. 2

c. 4

  1. CICH2 – CH2Br 2. CH3 – CHCI2 3. CH3 – CHBrCI 4. CH2Br – CHOH – CH3

    a. 1, 2, 3
    b. 1, 3, 4
    c. 2, 3, 4
    d. 3, 4

    d. 3, 4

    a. Cis-trans isomerism
    b. Functional group isomerism
    c. Positional isomerism
    d. Metamerism

    c. Positional isomerism

    a. ethanol and methoxy methane
    b. n-propyl alcohol and iso-propyl alcohol
    c. 1-butene and 2-butene
    d. none of the above

    a. ethanol and methoxy methane

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