Self Studies

Haloalkanes and Haloarenes Test 18

Result Self Studies

Haloalkanes and Haloarenes Test 18
  • Score

    -

    out of -
  • Rank

    -

    out of -
TIME Taken - -
Self Studies

SHARING IS CARING

If our Website helped you a little, then kindly spread our voice using Social Networks. Spread our word to your readers, friends, teachers, students & all those close ones who deserve to know what you know now.

Self Studies Self Studies
Weekly Quiz Competition
  • Question 1
    1 / -0

    Directions: In the following questions, A statement of Assertion (A) is followed by a statement of Reason (R). Mark the correct choice as.

    Assertion (A): Hydrolysis of (–)-2-bromooctane proceeds with inversion of configuration.
    Reason (R): This reaction proceeds through the formation of a carbocation.

    Solution

    Hydrolysis of (–)-2-bromooctane proceeds through the formation of a carbocation following SN1 reaction.

  • Question 2
    1 / -0

    Directions: In the following questions, A statement of Assertion (A) is followed by a statement of Reason (R). Mark the correct choice as.

    Assertion: Phosphorus chlorides (tri and penta) are preferred over thionyl chloride for the preparation of alkyl chlorides from alcohols.
    Reason: Phosphorus chlorides give pure alkyl halides.

    Solution

    Thionyl chloride is best halogen carrier to convert alcohol to alkyl halide because it gives by-products in gaseous state. Thus, we get pure alkyl halide in this reaction.

  • Question 3
    1 / -0

    Directions: In the following questions, A statement of Assertion (A) is followed by a statement of Reason (R). Mark the correct choice as.

    Assertion (A): In monohaloarenes, further electrophilic substitution occurs at ortho and para positions.
    Reason (R): Halogen atom is a ring deactivator.

    Solution

    Halogens are ortho-para directing due to (+M) or (+R) effect. Moreover, they are deactivating due to high electronegativity.

  • Question 4
    1 / -0

     Directions: In the following questions, A statement of Assertion (A) is followed by a statement of Reason (R). Mark the correct choice as.

    Assertion (A): Aryl iodides can be prepared by reaction of arenes with iodine in the presence of an oxidising agent.
    Reason (R): Oxidising agent oxidises I2 into HI.

    Solution

    Oxidising agent like (HIO3) converts HI to I2 otherwise HI may reduce aryl halide to arenes.
    5HI + HIO3 → 3H2O + 3I2

  • Question 5
    1 / -0

    Directions: In the following questions, A statement of Assertion (A) is followed by a statement of Reason (R). Mark the correct choice as.

    Assertion (A): Aryl halides undergo nucleophilic substitution reactions with ease.
    Reason(R): The carbon halogen bond in aryl halides has partial double bond character

    Solution

    Aryl halides are less reactive towards nucleophilic substitution reactions because of the carbon halogen bond in aryl halides has partial double bond character.

  • Question 6
    1 / -0

    Directions: In the following questions, A statement of Assertion (A) is followed by a statement of Reason (R). Mark the correct choice as.

    Assertion (A): tert-Butyl bromide undergoes Wurtz reaction to give 2, 2, 3, 3-tetramethylbutane.
    Reason (R): In Wurtz reaction, alkyl halides react with sodium in dry ether to give hydrocarbon containing double the number of carbon atoms present in the halide.

    Solution

    In Wurtz reaction, alkyl halides react with sodium in dry ether to give hydrocarbon containing double the number of carbon atoms present in the halide so tert-Butyl bromide undergoes Wurtz reaction to give 2, 2, 3, 3-tetramethylbutane.

  • Question 7
    1 / -0

    Directions: In the following questions, A statement of Assertion (A) is followed by a statement of Reason (R). Mark the correct choice as.

    Assertion (A): Presence of a nitro group at ortho or para position increases the reactivity of haloarenes towards nucleophilic substitution.
    Reason (R): Nitro group, being an electron withdrawing group decreases the electron density over the benzene ring.

    Solution

    Nitro group being an electron withdrawing group, decreases the electron density of benzene ring thus increasing the reactivity of haloarenes towards nucleophilic substitution.

  • Question 8
    1 / -0

    Directions: In the following questions, A statement of Assertion (A) is followed by a statement of Reason (R). Mark the correct choice as.

    Assertion (A): It is difficult to replace chlorine by –OH in chlorobenzene in comparison to that in chloroethane.
    Reason (R): Carbon-chlorine (C—Cl) bond in chlorobenzene has a partial double bond character due to resonance.

    Solution

    Chlorobenzene is very less reactive to nucleophilic substitution reaction by – OH group as Carbon-chlorine (C—Cl) bond in chlorobenzene has a partial double bond character due to resonance.

  • Question 9
    1 / -0

    Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

    Assertion : Alkylbenzene is not prepared by Friedel-Crafts alkylation of benzene.
    Reason : Alkyl halides are less reactive than acyl halides.

    Solution

    Alkyl halides give polyalkylation products.

  • Question 10
    1 / -0

    Directions: These questions consist of two statements, each printed as Assertion and Reason. While answering these questions, you are required to choose any one of the following four responses.

    Assertion : CHCl3 is stored in dark bottles.
    Reason : CHCl3 is oxidised in dark.

    Solution

    CHCl3 is stored in dark bottles to prevent oxidation of CHCl3 in the presence of sunlight.
     

Self Studies
User
Question Analysis
  • Correct -

  • Wrong -

  • Skipped -

My Perfomance
  • Score

    -

    out of -
  • Rank

    -

    out of -
Re-Attempt Weekly Quiz Competition
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