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11th And 12th > Chemistry

HYDROCARBONS MCQs

Total Questions : 30 | Page 1 of 3 pages
Question 1.


CH3CCHNaNH2−−−−XCH2CH2Br−−−−−−Y. Identify the product 'Y' is


  1.     Pent - 2 - ene
  2.     Pent - 2 - yne
  3.     Pent - 1 - yne
  4.     Pentane
 Discuss Question
Answer: Option B. -> Pent - 2 - yne
:
B

X is CH3CCNa+


Y is CH3CCCH2CH3


The first step removes the terminal hydrogen from the given substrate (reactant on the left). Such a removable hydrogen is called an acidic hydrogen. In the next step, the nucleophile - which is rich in electrons - attacks the CBr bond of ethyl bromide. Because of the difference in electronegativity between carbon and bromine, this CBr bond is polar - meaning, the bonding electrons are closer to the more electronegative bromine. This gives rise to the possibility of the carbon of the CBr bond having a slight deficit of electrons; let's just say that this carbon misses electrons and that is where the electron-rich terminal carbon of  CH3CC comes in. Hence, the reaction.


Question 2.


The polymer used as electrodes in batteries is


  1.     polythene
  2.     polypropene
  3.     polyacetylene
  4.     poly vinyl chloride
 Discuss Question
Answer: Option C. -> polyacetylene
:
C

A solid-state lithium/iodine battery has been formed by directly contacting metallic lithium with iodine-doped polyacetylene


Question 3.


Which of the following is correct order with respect to acidic nature :


  1.     CHCH>CH3CCH>CH2=CH2>CH3CH3
  2.     CHCH>CH2=CH2>CH3CCH>CH3CH3
  3.     CH2=CH2>CH3CH3>CHCH>CH3CCH
  4.     CH3CH3>CH3CCH>CH2=CH2>CHCH
 Discuss Question
Answer: Option A. -> CHCH>CH3CCH>CH2=CH2>CH3CH3
:
A

sp hybridized carbon hydrogen is more acidic as it is more electronegative.


Question 4.


Major product formed during the reaction between isobutyl bromide and benzene in presence of  anhydrous AlCl3 is :


  1.     isobutyl benzene
  2.     t- butyl benzene
  3.     n - butyl benzene
  4.     no reaction
 Discuss Question
Answer: Option B. -> t- butyl benzene
:
B

1,2 - methyl shift takes place in isobutyl carbonium ion


Question 5.


Assertion (A): - NO2 group is benzene ring deactivating and m - directing group


Reason (R): - NO2 group with draws electron density from benzene ring and makes ortho and para positions more electron deficient than meta position


  1.     A and R are true and R is the correct explanation of A
  2.     A and R are true and R is not the correct explanation of A
  3.     A is true, R is false
  4.     A is false but R is true
 Discuss Question
Answer: Option A. -> A and R are true and R is the correct explanation of A
:
A
The Meta directing nature of Nitro group can be seen through its resonance structures:
Assertion (A): - NO2 group Is Benzene Ring Deactivating And...
Question 6.



  1.     1,2 - Benzpyrene
  2.     1,2,5,6 -Dibenanthrecene
  3.     3 - Methyl anthracene
  4.     1,2 -Benzanthracene
 Discuss Question
Answer: Option D. -> 1,2 -Benzanthracene
:
D
You should be able to see that the 3 benzene rings at the bottom form an anthracene. 
And using the lowest locant rule, we can assign 1, 2 to the 2 carbons where benzene is attached.
So, the name would be 1,2-benzanthracene
Question 7.


The order of decreasing reactivity towards an electrophilic reagent for the following


I. Benzene             II. Toulene            III.  Chloro benzoic acid           IV.Phenol


  1.     IV > II > I > III 
  2.     I > II > III > IV  
  3.     II > IV > I > III  
  4.     IV > II > II > I  
 Discuss Question
Answer: Option A. -> IV > II > I > III 
:
A

OH group activates benezene ring more than - CH3 group


Question 8.


Energy barrier between staggered and eclipsed conformation of ethane is?


  1.     0.6K Cal/ mole
  2.     2.9 K Cal/ mole
  3.     12 K Cal/ mole
  4.     16 K Cal/ mole
 Discuss Question
Answer: Option B. -> 2.9 K Cal/ mole
:
B
Energy Barrier Between Staggered And Eclipsed Conformation O...
Question 9.


PhCCCH3H3O+/Hg+2−−−−−−−A. Then 'A' is 


  1.    
  2.    
  3.    
  4.    
 Discuss Question
Answer: Option A. ->
:
A

addition of water followed by tautomerism 


Question 10.


(CH3)3CHKMnO4−−−−A;CH3(CH2)2CH3HCl−−AlCl3B;CH3(CH2)4CH3Cr2O3,773K−−−−−−1020 atmC;


Correct statements are


A. 'A' remains same                      B. 'B' contains a 30 carbon


C. 'C' follows Huckel's rule            D. Both B and C are aromatic


  1.     A, B, C only
  2.     A, B, C ,D
  3.     A, C, D only
  4.     B, C only
 Discuss Question
Answer: Option A. -> A, B, C only
:
A
A does not undergo any change. There is no strong reason to support KMnO4 attacks a tertiary alkane to give an alcohol
B forms a tertiary alkane through isomerisation
C forms a benzene ring through aromatization reaction
 

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