Chemistry Chapter 13 Entry Test MCQs

Hybridization

a. 1 sigma and 1 pi bond
b. 3 sigma and 3 pi bond
c. 1 pi and 5 sigma bond
d. 1 pi and 3 sigma bond

c. 1 pi and 5 sigma bond

a. Sp3 hybridized
b. sp hybridized
c. Not hybridized
d. sp2 hybridized

b. sp hybridized

a. 1 σ and 1 π bond
b. 3 σ and 3 π bond
c. 1 π and 5 σ bond
d. 2 π and 3 σ bond

d. 2 π and 3 σ bond

a. Sp3 hybridized
b. sp hybridized
c. Not hybridized
d. sp2 hybridized

d. sp2 hybridized

a. sp > sp2 < sp3
b. sp > sp2 > sp3
c. sp < sp2 > sp3
d. sp < sp2 < sp3

d. sp < sp2 < sp3

a. sp > sp2 < sp3
b. sp > sp2 > sp3
c. sp < sp2 > sp3
d. sp < sp2 < sp3

d. sp < sp2 < sp3

Isomerism

a. Change in the valence of carbon
b. Change in the ratio of elements in compounds
c. Formation of double bond
d. Formation of branches in the chain of C atoms

d. Formation of branches in the chain of C atoms

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

a. 4

organic compound-chemistry

a. 1
b. 4
c. 3
d. 7

c. 3

a. Position isomerism
b. Metamerism
c. Tautomerism
d. Chain isomerism

a. Position isomerism

a. Geometric isomerism
b. Position isomerism
c. Chain isomerism
d. Metamerism

c. Chain isomerism

a. Functional group
b. Tautomers
c. Metamersim
d. Geometric

c. Metamersim

a. H3CHC = C(CH3)2
b. ClHC = CCl2
c. H3CHC = CClBr
d. H3CHC = CH2

c. H3CHC = CClBr

a. 6
b. 4
c. 7
d. 5

d. 5

a. C6H5 – CO – C6H5
b. C6H5–CO–CH2Cl
c. H – CO – CH3
d. C6H5–CO– CHCl2

a. C6H5 – CO – C6H5

a. 2-methyl-2-propanol
b. n-propyl-methyl ether
c. 2-butanone
d. 1-butanol

c. 2-butanone

a. Maleic acid and fumaric acid
b. Maleic acid and maleic anhydride
c. Ethylene dichloride and 1, 2-dichloroethene
d. None of these

a. Maleic acid and fumaric acid

Carbon

a. I and III
b. II and IV
c. III and IV
d. I and II

b. II and IV

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

b. 3

carbon-hydrogen-chemistry

a. Enantiomers
b. Diastereomers
c. Mesomers
d. Structural isomers

b. Diastereomers

a. 2
b. 0
c. 3
d. 1

b. 0

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

a. 5

a. 1,2-Dichloro-1-pentene
b. 1,1-Dichloro-1-pentene
c. 1,4-Dichloro-1-pentene
d. 1,3-Dichloro-1-pentene

b. 1,1-Dichloro-1-pentene

a. β-Bromobutyric acid
b. 1-Bromobutane
c. 1-Bromo-2-methylpropane
d. 2-Bromo-2-methylpropane

a. β-Bromobutyric acid

a. Functional group
b. Metamer
c. Position isomer
d. Tautomer

a. Functional group

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