12th class (Fsc) Chemistry unit 10 MCQs

a. They have an electrophilic carbon and a bad leaving group
b. They have an electrophilic carbon
c. They have a nucleophilic carbon and a good leaving group
d. They have an electrophilic carbon and a good leaving group

d. They have an electrophilic carbon and a good leaving group

a. The poncentration os substance as well as nucleophile
b. The concentration of substance
c. None of the above
d. The concentration of nucleophile

b. The concentration of substance

a. BF3
b. H2
c. NH3
d. H2S

a. BF3

a. Ter.butyl chloride
b. Iso-butyl bromide
c. N-butyl chloride
d. Sec. buyl halide

a. Ter.butyl chloride

a. One
b. Two
c. Four
d. Three

a. One

a. BF3
b. H2O
c. NH3
d. H2S

a. BF3

a. BF3
b. NH3
c. CI2
d. H2O

a. BF3

a. Strong acid
b. Lewis acid
c. Ether
d. Nucleophile

d. Nucleophile

a. Dsp3
b. Sp
c. Dsp2
d. Sp2

d. Sp2

a. Dsp3
b. Sp2
c. Sp
d. None of these

b. Sp2

a. 3rd order kinetics
b. 1st order kinetics
c. Zero order kinetics
d. 2nd order kinetics

d. 2nd order kinetics

a. 3rd
b. 1st
c. Zero
d. 2nd

d. 2nd

a. SN 1 and E2
b. E1 and E2
c. E1 and SN 1
d. E2 and SN2

a. SN 1 and E2

a. Second
b. Zero
c. Third
d. First

a. Second

a. Secondary alcohols
b. Primary alkyl halides
c. Primary alcohols
d. Secondary alkyl halides

d. Secondary alkyl halides

a. Proponal
b. Propane
c. Propanol
d. Propanoic acid

d. Propanoic acid

a. Denomination
b. Elimination
c. Reduction of benzene
d. Dehydration

b. Elimination

a. Oxidant
b. Lubricant
c. Plastic
d. Solvent

d. Solvent

a. KOH in alcohol
b. H2O at room temperature
c. Dilute NaOH(aq) warm
d. Ethanol, heat

c. Dilute NaOH(aq) warm

a. SN 1 mechanism
b. S2N mechanism
c. Both E1 and E2
d. Both SN1 and SN2

d. Both SN1 and SN2

a. RI>RBr>RCI>RF
b. RI>RBr>RF>RCI
c. RF>RBr>RCI>RI
d. RF>RCI>RBr>RI

d. RF>RCI>RBr>RI

a. 1,1,1-triflouro-2- bromo-2- chloroethane
b. 1-bromo-1- chloro-2,2,2- trifluroethane
c. 2-chloro-2- bromo-1,1,1- triflouromoethane
d. 2-bromo-2- chloro-1,1,1- trifluroethene

d. 2-bromo-2- chloro-1,1,1- trifluroethene

a. CH3 -CH2 -N2
b. CH3 -CH2 -NH- CH2 – CH3
c. H2 N-CH2 -CH2 – NH2
d. CH3 -CH2 -CH2 – NH2

d. CH3 -CH2 -CH2 – NH2

a. E1
b. E2
c. SN2
d. SN1

b. E2

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