CHM203




Category: CHM203

0

CHM203

1 / 55

A. Fused benzenoid hydrocarbon with three benzene rings is ________

2 / 55

B. Bleaching powder provides chlorine which oxidizes ethanol to _________.

3 / 55

C. Hydrogenation of benzene at higher temperature and under pressure yields ________

4 / 55

D. Hydrogen no - bond resonance is otherwise called _____________

5 / 55

E. The cannonical forms of  benzene were proposed by _____________

6 / 55

F. Reduction of benzene is by __________ of benzene.

7 / 55

G. The substitution of an acyl group into an aromatic ring by the reaction with an acid chloride in the presence of Lewis acid is called ____________

8 / 55

H. Another name for methyl benzene is __________

9 / 55

I. A benzenoid hydrocarbon in which two benzene rings are fused together at the ortho position is called ____________

10 / 55

J. Fused benzenoid hydrocarbons with two benzene rings is _________

11 / 55

K. The parent compound of polynuclear hydrocarbons is ___________

12 / 55

L. Down the group, electronegativity

13 / 55

M. The presence of an aromatic ring in a compound is detected by ____________

14 / 55

N. Naphthalene has ________ number of resonance hybrid structures

15 / 55

O. Solubility of branched isomers is __________ than that of straight chain isomers

16 / 55

P. In terms of steric effect,  conformational isomer is __________ more stable.

17 / 55

Q. Inductive effect is a type of ____________ effect

18 / 55

R. The method of reduction of the carbonyl group of ketone produced by Friedel -crafts acylation is ------------ reduction.

19 / 55

S. The number or π-electrons in benzene is _____________

20 / 55

T. An example of Isolated Benzenoid Hydrocarbon is __________

21 / 55

U. The definition of an acid as a proton donor was given by ________

22 / 55

V. Oxidation of naphthalene under controlled condition yields ___________

23 / 55

W. Cyclohexane has _______ fewer hydrogens than nhexane.

24 / 55

X. A side reaction that occurs during substitution reactions of alkyl halides is _________

 

25 / 55

Y. Tautomers which differ from each other only in the location of a hydrogen atom and a double bond are called ____________

26 / 55

Z. Two factors that affect the boiling point of a substance are ________ and _________

27 / 55

AA. The influence of the inductive effect on acid strength is almost negligible after the __________ carbon in the chain.

28 / 55

AB. The effect arising from the spatial interactions between the groups in a compound is called _____________

29 / 55

AC. The method of reduction of the carbonyl group of ketone produced by Friedel - craft is __________

30 / 55

AD. Branched chain hydrocarbons have lower __________ than their straight chain isomers.

31 / 55

AE. A change in molecular structure which affect the reactivity of the molecule by changing the electron distribution is called __________

32 / 55

AF. The types of geometric isomers are trans and __________

33 / 55

AG. In electrophilic addition to alkenes, the electrophilic attack is on __________

34 / 55

AH. The process by which benzene and its derivatives are extracted from petroleum is called ___________

35 / 55

AI. The reaction in which aryl halides are formed from aromatic amines is called _________

36 / 55

AJ. The amount of substance dissolved in a certain amount of solvent is referred to as ___________

37 / 55

AK. In terms of steric effect _________ geometric isomer is more stable.

38 / 55

AL. Unbranched isomer has higher _________ than branched isomer

39 / 55

AM. In terms of steric effect _________ geometric isomer is more stable.

40 / 55

AN. The major product in the nitration of nitrobenzene is ____________

41 / 55

AO. The dehydrohalogenation of alkyl halides yields __________

42 / 55

AP. The type of tautomerism which involves a shift in interatomic distance within a molecule, without the separation of any atom from the rest of the molecule , as an intermediate stage is called ____________

43 / 55

AQ. The stronger an acid the ___________ is its conjugate base

44 / 55

AR. In keto-enol tautomers, the tautomer that predominates is __________

45 / 55

AS. There are ---------- resonance structures of benzene

46 / 55

AT. For halogen derivatives of aromatic compounds, boiling point ---------- with increase in atomic size of the halogen atom.

47 / 55

AU. In terms of aromatization, naphthalene has ___________ π electrons

48 / 55

AV. The E2 reactions of alkyl halides are favoured by the use of __________

49 / 55

AW. The most widely used method for the preparation of alkyl halides is from __________

50 / 55

AX. The benzenoid hydrocarbons in which two or more benzene rings are fused together at ortho position in such a way that each pair of rings shares rings shares two carbons are called ---------- benzenoid hydrocarbon.

51 / 55

AY. The rule that states that in a dehydrohalogenation reaction of alkyl halides, the major product will be the product that has the more alkyl groups attached to the resultant carbon - carbon double bond is __________ rule.

52 / 55

AZ. Reduction of benzene using Nickel at 425-525K and 25atm yields __________

53 / 55

BA. The backbone of an organic molecule is __________

54 / 55

BB. The extent to which acids transfer a proton to a standard base determines __________

55 / 55

BC. Sulphonation of benzene yields ___________

Rate this quiz




Hello NOUNITES! Join other NOUNITES on Whatsapp and Telegram below, EXCLUSIVE UPDATES awaits you from various study centres and happenings in NOUN. Stay updated
 
Don't miss out, JOIN OVER 22,000 other students already following our platforms

FOLLOW WHATSAPP CHANNEL  FOLLOW TELEGRAM CHANNEL 
    
JOIN WHATSAPP GROUP   JOIN TELEGRAM GROUP
close-link