Home
Class 11
CHEMISTRY
Assertion. Acetylene reacts with sodamid...

Assertion. Acetylene reacts with sodamide te evolve `H_2` gas
Reason. Acetylene is a weaker acid than ammonia

A

If both assertion and reason are true, and reason is the true explanation of the assertion.

B

If both assertion and reason are true, but reason is not the true explanation of the assertion.

C

If assertion is true, but reason is false.

D

If both assertion and reason are false

Text Solution

AI Generated Solution

The correct Answer is:
To solve the question, we need to analyze both the assertion and the reason provided. ### Step 1: Understanding the Assertion The assertion states that acetylene reacts with sodamide to evolve hydrogen gas (H₂). - **Acetylene (C₂H₂)** has a structure of H-C≡C-H, where the carbon atoms are sp-hybridized. - **Sodamide (NaNH₂)** is a strong base and can deprotonate acetylene. When acetylene reacts with sodamide, the hydrogen atom attached to the carbon is acidic enough to be removed by the strong base, resulting in the formation of sodium acetylide (NaC≡C) and ammonia (NH₃). The reaction can be represented as: \[ \text{C}_2\text{H}_2 + \text{NaNH}_2 \rightarrow \text{NaC}_2\text{H} + \text{NH}_3 \] This reaction indeed evolves hydrogen gas, confirming the assertion is correct. ### Step 2: Understanding the Reason The reason states that acetylene is a weaker acid than ammonia. - **Acidity** is determined by the stability of the conjugate base formed after deprotonation. - When acetylene loses a hydrogen ion (H⁺), it forms the acetylide ion (C≡C⁻). When ammonia loses a hydrogen ion, it forms the amide ion (NH₂⁻). To compare their acidity: 1. The conjugate base of acetylene (C≡C⁻) is relatively stable due to the sp-hybridization of the carbon atom, which holds the negative charge more effectively. 2. The conjugate base of ammonia (NH₂⁻) is less stable because the negative charge is held by a less electronegative atom (nitrogen) compared to carbon. Thus, acetylene is actually a stronger acid than ammonia, making the reason incorrect. ### Conclusion - The assertion is correct: Acetylene reacts with sodamide to evolve hydrogen gas. - The reason is incorrect: Acetylene is not a weaker acid than ammonia; it is actually a stronger acid. ### Final Answer The assertion is correct, but the reason is incorrect. ---

To solve the question, we need to analyze both the assertion and the reason provided. ### Step 1: Understanding the Assertion The assertion states that acetylene reacts with sodamide to evolve hydrogen gas (H₂). - **Acetylene (C₂H₂)** has a structure of H-C≡C-H, where the carbon atoms are sp-hybridized. - **Sodamide (NaNH₂)** is a strong base and can deprotonate acetylene. ...
Promotional Banner

Topper's Solved these Questions

  • HYDROCARBONS

    PRADEEP|Exercise Competition Focus (JEE(main and advanced)/Medical Entrance) VII.NUMERICAL VALUE TYPE QUESTIONS|1 Videos
  • EQUILIBRIUM IN PHYSICAL AND CHEMICAL PROCESSES

    PRADEEP|Exercise Competition Focus (Jee(Main and advanced)/Medical Entrance) VIII. ASSERTION - REASON TYPE QUESTIONS (TYPE - II)|10 Videos
  • HYDROGEN

    PRADEEP|Exercise COMPETITION FOCUS (Assertion-Reason Type Questions) Type 2|15 Videos

Similar Questions

Explore conceptually related problems

Assertion : Asetylene on reacting with sodamide gives sodium acetylide and ammonia. Reason : ap hybridised carbon atoms of acetylene are considerably electronegative .

Assertion : Acetylene on reacting with sodamide gives sodium acetylide and ammonic. Reason : sp- hybridised carbon atoms of acetylene are considerably electronegative.

Assertion (A): Sn reacts with HCl to produce H_(2) gas. Reason (R ): Sn is a better reducing agent than H_(2) gas.

Assertion : Acetylene is more acidic than ethylene. Reason : Acetylene has sp character of carbon and, therefore, more s-character.

PRADEEP-HYDROCARBONS-Competition Focus (JEE(main and advanced)/Medical Entrance) VIII. ASSERTION - REASON TYPE QUESTIONS
  1. Assertion. Addition of HI to vinyl chloride produces -chloro-1-todoeth...

    Text Solution

    |

  2. Assertion. Propene reacts with hydrogen chloride in presence of organi...

    Text Solution

    |

  3. Assertion. C-H bond in ethyne is shorter than C-H bonds in ethene. ...

    Text Solution

    |

  4. Assertion. Calcium carbide on hydrolysis gives ethylene Reason. Cal...

    Text Solution

    |

  5. Assertion. Acidity of the C-H bond decreases in the order: HC-=CH gt H...

    Text Solution

    |

  6. Assertion. Acetylene reacts with sodamide te evolve H2 gas Reason. ...

    Text Solution

    |

  7. Assertion : Acetylene on reacting with sodamide gives sodium acetylide...

    Text Solution

    |

  8. Assertion. Addition of H2O to acetylene occurs in presence of dil. H2S...

    Text Solution

    |

  9. Assertion. But 1-yne and but-2-yne can be distinguished by ammoniacal ...

    Text Solution

    |

  10. Assertion. Alkynes are more reactive towards nucleophilic addition rea...

    Text Solution

    |

  11. Assertion : 2-butyne on controlled hydrogenation with Pd/CaCO3 in pre...

    Text Solution

    |

  12. Assertion. But-2-yne on reduction with Na//NH3(l) gives trans-2-buten...

    Text Solution

    |

  13. Assertion. Benzene does not decolourize Br2- water Reason. Benzene ...

    Text Solution

    |

  14. Assertion. Tropylium cation is aromatic in nature Reason. The on...

    Text Solution

    |

  15. Assertion : Cyclopentadienyl anion is much more stable than allyl anio...

    Text Solution

    |

  16. Assertion: Friedel-Crafts reaction is used to introduce an alkyl or ac...

    Text Solution

    |

  17. Assertion (A) Friedel - Crafts reaction benzene with n - propyl chlori...

    Text Solution

    |

  18. Assertion : Alkyl benzene is not prepared by Friedel- Crafts alkylatio...

    Text Solution

    |

  19. Assertion : Oxidation of toluene as well as ethyl benzene with KMnO(4)...

    Text Solution

    |

  20. (A) Rate of nitration of benzene and hexadeuterobenzene are different....

    Text Solution

    |