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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
206
times
Last played on Dec 10, 2016View comments
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Sample Questions

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