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AIEEE Chemistry (2005)

AIEEE Chemistry (2005)
Created by Quizmagic Team on Jan 09, 2013 06:42 PM.
There are 25 questions of AIEEE Chemistry examination of year 2005 in this quiz. Take this quiz with previous year questions and improve your Chemistry for this competitive examination
Top 5 Scores
Anonymous
91
00:42
Anonymous
82
01:15
Anonymous
80
02:34
Molu Nair
77
00:56
Anonymous
77
01:11
Questions
25
Minutes
15
High Score
91
00:42
Quiz Played
216
times
Last played on Jun 22, 2017View comments
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Sample Questions

Question 1
Elimination of bromine from 2-bromobutane results in the formation of-
predominantly 1-butene
predominantly 2-butyne
predominantly 2-butene
equimolar mixture of 1 and 2-butene
Question 2
Which types of isomerism is shown by 2,3-dichlorobutane?
Geometric
Structural
Optical
Diastereo
Question 3
Amongst the following the most basic compound is
acetanilide
p-nitroaniline
benzylamine
aniline
Question 4
Acid catalyzed hydration of alkenes except ethene leads to the formation of
mixture of secondary and tertiary alcohols
mixture of primary and secondary alcohols
primary alcohol
secondary or tertiary alcohol
Question 5
Alkyl halides react with dialkyl copper reagents to give
alkenes
alkenyl halides
alkyl copper halides
alkanes
Question 6
Of the five isomeric hexanes, the isomer which can give two monochlorinatedcompounds is
2-methylpentane
n-hexane
2,2-dimethylbutane
2, 3-dimethylbutane
Question 7
Which of the following is fully fluorinated polymer?
Neoprene
Teflon
PVC
Thiokol
Question 8
Which one of the following methods is neither meant for the synthesis nor for separation of amines?
Wurtz reaction
Curtius reaction
Hofmann method
Hinsberg method
Question 9
Reaction of one molecule of HBr with one molecule of 1,3-butadiene at 400C gives predominantly
1-bromo-2-butene under thermodymically controlled conditions
3-bromobutene under kinetically controlled conditions
3-bromobutene under thermodynamically controlled conditions
1-bromo-2-butene under kinetically controlled conditions
Question 10
Tertiary alkyl halides are practically inert to substitution by SN2 mechanism because of
insolubility
inductive effect
instability
steric hindrance
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