→Moist Ag2O (A) product
Major product (A) is:
→KCN Product of reaction is:
(MOM chloride)
(Methoxy methyl chloride)
Me-O-CH2-CH2-CN
CN -CH2-CN
Alkyl halides can be obtained by all methods except:
CH3CH2OH + HCl/ZnCl2 →
CH3-CH2-CH3-CH2 →Cl2/UV light
C2H5OH + NaCl →
CH3COOAg + Br2/CCl4 →
In order to prepare 1-chloropropane, which of the following reactants can be employed?
Propene and Cl2 followed by treatment with aq. KOH
Propanol-1 and SOCl2/pyridine
Any of the above can be used
Which of the following molecules would have a carbon-halogen bond most susceptible to nucleophilic substitution ?
2-Fluorobutane
2-Chlorobutane
2-Bromobutane
2-Iodobutane
When benzyl chloride is treated with ethanolic KCN, the major product formed is:-
benzyl alcohol
benzyl cyanide
benzyl isocyanide
Grignard reagent shows addition on:
>C=O
-C≡N
>C=S
all of these
Pick up the correct statement about alkyl halides:-
They show H-bonding.
They are soluble in water.
They are soluble in organic solvents.
They do not contain any polar bond.
Chlorination of CS2 gives:
CCl4
CS2Cl2
CH4
CHCl3
Sodium ethoxide reacts with ethyl iodide to yield:
CH3CH3
C2H5OCH3
C2H5OC2H5
none of these
Which set of reagents will produce freon (CCl2F2)?
C + F2 + Cl2 →
CH3Cl + F2 →
CCl4 + HF →SbCl5
CCl4 + F2 →
Chloroform is kept in dark-colored bottles because:-
It is inflammable
It gives a peroxide
It undergoes rapid chlorination
It is oxidized to poisonous phosgene
Which statement is correct ?
C2H5Br reacts with alcoholic KOH to form C2H5OH
C2H5Br when treated with metallic sodium gives ethane
C2H5Br when treated with sodium ethoxide forms diethyl ether
C2H5Br with AgCN forms ethyl cyanide
CH3NH2 reacts with CH3MgX to give:
ethane
acetone
alcohol
methane
Ethylidine dichloride (CH3CHCl2) can be prepared by the addition of hydrogen chloride on:
C2H6
C2H4
C2H2
The reactivity order of alkyl halides depends upon:
Nature of alkyl group only
Nature of halogen atom only
Nature of both alkyl group and a halogen atom
None of the above
An alkyl iodide on standing darkens, due to:
hydrolysis
conversion into ether
liberation of iodine
formation of alkanes
The given reaction is an example of,
C2H5Br + aqu. KCN → C2H5CN + KBr
Elimination
Nucleophilic substitution
Electrophilic substitution
Redox change
In the following sequences of reactions;
CH3CH2CH2Br →-HBrKOH(alc.)(A) →HBr (B) →KOH(aq) (C)
the product (C) is:
propene
propyne
propan-1-ol
propan-2-ol
Chloroform on reduction with Zn and HCl (alc.) gives:-
formic acid
chloretone
chloropicrin
methylene dichloride
Westrosol is:-
acetylene tetrachloride
acetylene dichloride
trichloroehyne
1,1,2-trichloroethene
Reagent not used to prepare an alkyl halide from an alcohol is:
HCl+ ZnCl2
NaCl
PCl5
SOCl2
Most readily hydrolysed halide is:-
C6H5Cl
(C6H5)2CHCl
C6H5CH2Cl
(C6H5)3CCl
CCl4 is insoluble in water because:-
water is non-polar
CCl4 is non-polar
water and CCl4 are polar
none of the above
In the reaction,
CH3C≡C¯Na+ + (CH3)2CHCl → ...............
the product formed is:
4-Methylpent-2-yne
propyne and propene
Chloral is:
CCl3 CHO
CCl3COCH3
CCl3CO-CCl3
CCl3CH2OH
A compound A of formula C3H6Cl2 on reaction with alkali can give B of formula C3H6O or C of formula C3H4. B on oxidation gave a compound of the formula C3H6O2. C with dilute H2SO4 containing Hg2+ ion gave D of formula C3H6O, which with bromine and NaOH gave the sodium salt of C2H4O2. Then A is:
CH3CH2CHCl2
CH3CCl2CH3
CH3CHClCH2Cl
CH2ClCH2CH2Cl
Ethylene on treatment with chlorine gives:-
Ethylene dichloride
Ethylene chlorohydrin
The compound A forms B with sodium metal and again A forms C with PCl5, but B and C form diethyl ether. Thus A, B and C are:
C2H5OH, C2H5ONa , C2H5Cl
C2H5OH, C2H5Cl, C2H5ONa
C2H5OH, C2H5Cl, C2H4Cl2
The halide which undergoes nucleophilic substitution most readily is:
p-H3CC6H4Cl
o-H3COC6H4Cl
p-ClC6H4Cl
p-O2NC6H4Cl
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