1 |
To prepare ethane by Wurtz synthesis the suitable alkyl halide is |
Ethyl iodide
any alkyl iodide
Ethyl chloride
Methyl bromide
|
2 |
Reaction of ethyl bromide with ammonia |
<div>Completes in a single step</div><div><br></div>
Completes in two steps
Continues till N is left with no lone pair
is reversible
|
3 |
In beta elimination reaction |
carbon number changes
unsaturated compound is formed
hybridization. ofC remains same
pi bonds are decreased
|
4 |
Which is an intermediate in SN1 reaction |
Ethoxide ion
Carbocation
alkyl halide
alkene
|
5 |
The reagent for alkaline hydrolysis of ethyl bromide to form ethyl alcohol is |
water at room T
Alcoholic KOH+heat
Ethanol + heat
dil. NaOH+ heat
|
6 |
Which pair gives same dehydrohalogenation product |
<div>I-Chlorobutane, 2-Chlorobutane</div><div><br></div>
I-Chloropropane, 2-Chloropropane
I-Bromopentane. 3-Bromopentane
iso-butvl chloride. 2°- butyl chloride
|
7 |
In an elimination reaction a more substituted alkene is formed due to the stability associated with |
Free radical
transition state
Activated complex
Carbocation
|
8 |
Dehydrohalogenation of secondary butyI bromide will give |
Propene
1-Butene
Butene
2-Butene
|
9 |
Which of the following reactants will be required to form ethene from ethyl chloride |
<sub>Alcoholic KOH</sub>
Alkaline KMnO4
Aqucous KOH
Aqucous NaOH
|
10 |
Which one among the following is not a good leaving group |
HSO4-
CI-
OH-
Br-
|
11 |
In nucleophilie substitution bimolecular reaction the order of reaction with respect to substrate |
2 order
3 order
1st order
Zero order
|
12 |
Which compound is obtained hy the elimination reaction on bromoethane? |
Butene
Ethene
Propene
Propane
|
13 |
When 2-bromobutane reacts with alcoholic KOH, the reaction is called |
Chlorination
Halogenation
Dehydrohalogenation
Hydrogenation
|
14 |
Which of the following alkyl halides undergoes SN1 reaction fastest |
Methyl chloride
Isobutyl chlorido
Ethy l chloride
Tertiary butyl chloride
|
15 |
A mixture of 1-chloropropane and 2-chloro-propane when treated with alcoholic KOH, gives |
Prop-2-ene
Isopropy lene
Propene
A mixture of prop-l-ene
|
16 |
In elimination reaction i.e, in the formation of alkene, the reactivity of alkyl halide is in the order: |
CI>Br>I
I>Br>Cl
Br>CI>I
I>CI> Br
|
17 |
The species which are produced by heterolytic bond breaking and can act as electron pair donor |
Free radicals
Cations
Nucleophiles
electrophile
|
18 |
Among the following, which one is nucleophile |
H+
Ca2+
OH-
Na+
|
19 |
Which is an intermediate in Svl |
Ethoxide ion
Alkene
Alkyl halide
Carbocation
|
20 |
Which one of the following is NOT a nucleophile |
NH2+
BF3
H2O
CH3-
|
21 |
The order of reactivitv of alksI halides towards nucleophile is |
RI>RBr RF>RCI
RF>RCI>RBr>RI
RI>RBr> RCI>RE
RF>RBr>RCI>RI
|
22 |
The alkaline hydrolysis of bromoethane shown below gives alcohol as the product: H3C-CH2-Br-------H3C-CH2-OH The reagent and the condition used in this reaction may be: |
H20 at room temperature
KOH in alcohol
Ethanol. heat
Dilute NaOH(aq) warm
|
23 |
When purely alcoholic solution of sodium/potassiumhydroxide and halogenoalkanes are reacted an alkene is formed, what is the mechanism of reaction? |
Elimination
Debromination
Dehydration
Reduction
|
24 |
Correct order for the reactivity ofalkyl halide in S, reactions |
R-I>R-F>R-CI
R-F>R-CI>R-I
R-I>R-CI>R-F
R-CI>R-I>R-F
|
25 |
Correct statement about Nucleophilic substitution bimolecular is |
Transition state is formed
Inversion take place
It is two step reacticn
Both a &c
|
26 |
The reaction C2H5CI + aqueous KOH---------C2H5OH+ KCI is |
Electrophilic addition
Nucleophilic addition
Electrophilic substitution
Nucleophilic substitution
|
27 |
An alkyl halide reacts with NH3 to give |
Amide
Cyanide
Amine
Aniline
|
28 |
Out of monochloro, monobromo and mongiodo derivatives of ethane, the mos reactive compound towards nucleophilic substitution will be |
C2H5Br
C2H5Cl
C2H5I
All are equally reactive
|
29 |
Elimination unimolecular reactions involve |
Second order kinetics
First order kinetics
Third order kinetics
Zero order kinetics
|
30 |
Which of the following is primary alkyl halide |
IsopropyI halide
Sec-butyl halide
Tert-buryi halide
Neo-pentyl halide
|
31 |
Which isomer of C4H9Br will produce 2-methyl propane-2-ol on treatment with aqueous KOH |
n-butyI bromide
Sec-butyI bromide
Isobutyl halide
Tertiary butyl chloride
|
32 |
Which one of the following is not associated with SN2 mechanism |
100 % inversion of configuration
Tertiar alkyI halides
2nd order kinetics
Change of hy bridization from sp³ to sp² in transition state
|
33 |
Which of the following factors does not affect the SN1 rate is |
Nucleophilicity of the attacking nucleophile
Stability of the carbonium ion
Solvent system
The nature of leaving group
|
34 |
In the transition state of S2 mechanism reaction with alkyl halides, which of the following orbital hybridization is involved |
sp³
sp
sp²
dsp³
|
35 |
Which of the following decides the reactivity of alkyl halides? |
C-C bond strength
C-H bond strength
C-X bond strength
Electronegativity difference
|
36 |
Chloroform (CHCl3) is? |
Primary alkyl halide
Secondary alkyl halide
Tertiary alkyl halide
a liquid
|
37 |
Which is a good nucleophile as well as a good leaving group? |
F-
Cl-
Br-
I-
|
38 |
An amine is produced in the following reaction C2H5l+2NH3-------C2H5NH2 +NH4l. What is mechanism? |
Electrophilic addition
Electrophilic substitution
Nucleophilic addition
Nucleophilic substitution
|
39 |
The Sl mechanism for the hydrolysis of an alkyl halide to an alcohol involves the formation of |
Carbocation
Carbanion
Pentavalent carbon in the transition state
Free radical
|
40 |
SN2-reactions can be usually observed in |
Primary alkylı halide
secondary alkyl halide
Tertiary alkyl halide
Both A. and B
|
41 |
Alkyl halides are considered to be very reactive compounds towards nucleophiles, because |
The have an electrophilic carbon
They have an electrophilic carbon and a bad leaving group
They have an electrophilic carbon and a good laving group
They have a nucleophilic carbon and a good leaving group
|
42 |
The rate of E1 reaction depends upon |
The concentration of substrate
The concentration of substrate as well as nucleophile
The concentration Nucleophilic
Nature of Catalyst
|
43 |
For which mechanisms, the first step involved is the same |
E1 and E2
E2 and SN2
E2 and E1
E1 and SN1
|
44 |
The average bond energy of C-Br is |
228 kJmol-1
250 kJmol-1
200 kJmol-1
290 kJmol-1
|
45 |
The carbon atom of an alkyl group attached with halogen atom is called |
Electrophile
Free redical
Nucleophile
Nucleophilic centre
|
46 |
Hydration of ethene is an example of |
Electrophilic addition
Electrophilic substitution
Nucleophilic addition
Nucleophilic substitution
|
47 |
Ethyl and methyl groups are equidistant in a chain, the preference is given to? |
Ethyl
methyl
both ethyl and methyl
methyl mostly
|
48 |
Tertiary alcohols are the easiest to dehydrate because |
They form stable carbocation
They have less hydrogen
They have bigger size
They are polar
|
49 |
The reaction of alkyl halide in the presence of alcoholic KOH is |
Substitution
Addition
Acid-base
Elimination
|
50 |
Which group activates the benzene ring |
-COOH
-COR
-CHO
-OH
|
51 |
Benzene reacts with Ethyl chloride in presence of AICls to give |
Benzalchloride
Benzyl chloride
Ethyl benzene
Benzotrichloride
|
52 |
Ethene can give all of the following reactions except |
Addition
Free radical substitution
Hydrohalogenation
Hydration
|
53 |
Active sulphonating agent during sulphonation of benzene is |
SO2
SO3
SO3H
SO3+
|
54 |
Glyoxal molecule has? |
two carbonyl groups
One aldehydic and one carbonyl group
Two aldehydic groups
Two carboxyl group
|
55 |
Ethane when completely halogenated in excess of chiorine can form |
Hexachloroethane
Dichloroethane
Pentachloroethane
1.1.2.2-terachloroethane
|
56 |
The origin ofacidic nature of alkyne is? |
small size of C
Small size of H
polarity of triple bond
sp hybridization
|
57 |
A compound that has a nucleophilic carbon? |
C2H2
C2H4
C3H8
C6H6
|
58 |
The addition of HCI to ethene gives? |
Chloroethane
1,2-dichloroethane
1.1-dichloroethane
2-chloroethane
|
59 |
The reaction that generates an ionic bond is |
Halogenation of ethene
polymerization of ethene
Hydrogenation of ethyne
Reaction of ethyne withs sodamide
|
60 |
Acetylide can give back ethyne upon treatment with |
water
strong base
dil. Acid
weak base
|