EASY
Earn 100

Arrange the following alkyl halides in order of dehydrohalogenation; C2H5I, C2H5Cl, C2H5F

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Important Questions on Haloalkanes and Haloarenes

HARD
Which of the following is the most correct electron displacement for a nucleophile reaction to take place?
EASY
For a given alkyl group, the reactivity order of halides in SN1 reaction is
MEDIUM
The compound A on reaction with chlorine in presence of u.v. light gives B; which when reacted with AgNO2 in the solvent N, N-dimethylformamide, gives 2-Nitrobutane. The compound A is
MEDIUM
Which of the following has the highest dipole moment?
HARD
The dipole moment of chlorobenzene is lower than that of cyclohexyl chloride. Explain.
EASY
The synthesis of alkyl fluorides is best accomplished by:
EASY
How do the bond lengths of C-X  bonds (X=F, Cl, Br, I) in haloalkanes vary and why?
EASY
The correct pair(s) of the ambident nucleophiles is (are):
(A) AgCN/KCN
(B) RCOOAg/RCOOK
(C) AgNO2/KNO2
(D) AgI/KI
EASY
Which of the following statements is true in the case of alkyl halides?
HARD
Explain why alkyl halides, though polar, are immiscible with water?
EASY
Consider the reaction
CH3CH2CH2Br+NaCNCH3CH2CH2CN+NaBr
This reaction will be the fastest in
MEDIUM
Which of the following will most readily give the dehydrohalogenation product?
EASY
The conversion of ethyl bromide to ethyl iodide using sodium and dry acetone, this reaction is known as
EASY
The correct sequence of bond enthalpy of ' $\mathrm{C}-\mathrm{X}$ bond is:
EASY
For the compounds CH3Cl, CH3Br, CH3I and CH3F, the correct order of increasing C-halogen bond length is :