Self Studies
Self Studies
Self Studies
Self Studies

Haloalkanes & H...

TIME LEFT -
  • Question 1
    1 / -0.25

    Only One Option Correct Type

    Direction (Q. Nos. 1-5) This section contains 5 multiple choice questions. Each question has four choices (a), (b), (c) and (d), out of which ONLY ONE option is correct.

    Q. 

    What is the major alkene product in the following reaction?

  • Question 2
    1 / -0.25

    Which of the following gives 1-butene as the major product most easily on heating with AgOH?

  • Question 3
    1 / -0.25

    1-butene would be formed most easily in the following reaction when X is

  • Question 4
    1 / -0.25

    Which of the following compound is most likely to follow E1 cb mechanism when treated with C2 H5 ONa in ethanol?

  • Question 5
    1 / -0.25

    Consider the following reaction and the product formed.

    Q. 

    The most likely mechanism of the above reaction is

  • Question 6
    1 / -0.25

     

    One or More than One Options Correct Type

    Direction (Q. Nos. 6-8) This section contains 3 multiple choice questions. Each question has four choices (a), (b), (c) and (d), out of which ONE or MORE THAN ONE are correct.

    Q. 

    Which of the following gives methanol as the major product when heated with AgOH?

     

  • Question 7
    1 / -0.25

     

    Which of the following gives cis-2,3-diphenyl, 1-2-butene as the major E2 product, when treated with ethanolic KOH solution?

     

  • Question 8
    1 / -0.25

     

    The following elimination reaction, if proceeds by E1cb mechanism, equilibrium mixture would consist of

     

  • Question 9
    1 / -0.25

     

    Comprehension Type

    Direction : This section contains 2 paragraphs, each describing theory, experiments, data, etc. Each question has only one correct answer among the four given options (a), (b), (c) and (d).

    Passage I

    The following E2 is carried out with different halogen substituent:

    From the percentage yield of two products observed with different leaving group, it was concluded that both ease of leaving group and steric hindrance to the approach of base CH3 O-  to β-H affect the orientation of elimination reaction.

    Q. 

    Based to the above observation, which flask will have the largest amount of 1-hexene?

     

  • Question 10
    1 / -0.25

    Passage I

    The following E2 is carried out with different halogen substituent:

    From the percentage yield of two products observed with different leaving group, it was concluded that both ease of leaving group and steric hindrance to the approach of base CH3 O-  to β-H affect the orientation of elimination reaction.

    Q. 

    Highest percentage yield of 1-hexene in flask 4 leads us to conclude that

Submit Test
Self Studies
User
Question Analysis

  • Answered - 0

  • Unanswered - 10

  • 1
  • 2
  • 3
  • 4
  • 5
  • 6
  • 7
  • 8
  • 9
  • 10
Submit Test
Self Studies Get latest Exam Updates
& Study Material Alerts!
No, Thanks
Self Studies
Click on Allow to receive notifications
Allow Notification
Self Studies
Self Studies Self Studies
To enable notifications follow this 2 steps:
  • First Click on Secure Icon Self Studies
  • Second click on the toggle icon
Allow Notification
Get latest Exam Updates & FREE Study Material Alerts!
Self Studies ×
Open Now