The chelating ligand used to remove excess of copper and iron in chelate therapy is
D-penicillamine
oxalate ion
EDTA
ethylenediamine
The correct decreasing order of reactivity for a given alkyl (R) group in both SN1 and SN2 reaction mechanisms is
R - I > R - Br > R - Cl > R - F
R - I > R - Cl > R - Br > R - F
R - F > R - Cl > R - Br > R - I
R - F > R - I > R - Cl > R - Br
Chloroform reacts with oxygen in the presence of light to give
carbon tetrachloride
carbonyl chloride
methyl chloride
acetaldehyde
Which one of the following is not expected to undergo iodoform reaction?
Propan-2-ol
Diphenyl methanol
1-phenylethanol
2-butanol
Which one of the following halogen compounds is difficult to be hydrolysed by SN1 mechanism?
Tertiary butyl chloride
lsopropyl chloride
Benzyl chloride
Chlorobenzene
Which one of the following is not an allylic halide?
4-bromopent-2-ene
3-bromo-2-methylbut-1-ene
1-bromobut-2-ene
4-bromobyt-1-ene
Excess of copper in toxic proportions in plants/animals can be removed by chelating with
EDTA
ethane-1,2-diamine
oxalate ion
D-pencillamine
Which will undergo SN2 reaction fastest among the following halogen compounds?
CH3CH2F
CH3CH2Cl
CH3CH2Br
CH3CH2I
D.
CH3CH2I
SN2 reactions involve the formation of intermediate transition state, thus less hindered alkyl halide readily undergoes this reaction.
Moreover, C-I bond is less stable than C-Br or C-Cl bond, thus alkyl iodides are more reactive as compared to other halides. Hence, CH3CH2I is most reactive towards SN2 reaction.
The alkyl halide that undergoes SN1 reaction more readily is
t-butyl bromide
n-propyl bromide
vinyl bromide
isopropyl bromide
An alkyl halide (R X) reacts with Na to form 4, 5-diethyloctane. Compound R X is
CH3(CH2)3Br
CH3(CH2)2CH(Br)CH2CH3
CH3(CH2)3CH(Br)CH3
CH3(CH2)5Br