Home
Class 11
CHEMISTRY
The correct trend of acidic nature of th...

The correct trend of acidic nature of the following alkynes is

A

`CH-=CH gt CH_(3) - C-=CH gt CH_(3) C -=C CH_(3)`

B

`CH_(3)-C -=CH gt CH -= CH gt CH_(3) C -= C CH_(3)`

C

`CH_(3)C -= C CH_(3) gt CH_(3 - C-=CH gt CH -= CH`

D

`CH-=CH gt CH_(3)C -= C CH_(3) gt CH_(3) C -=CH`

Text Solution

AI Generated Solution

The correct Answer is:
To determine the correct trend of acidic nature among the given alkynes, we need to analyze the factors that affect the acidity of alkynes. Here’s a step-by-step solution: ### Step 1: Understand the Factors Affecting Acidity The acidity of alkynes is influenced primarily by two factors: 1. **Inductive Effect (+I effect)**: Electron-donating groups increase electron density at the carbon atom of the alkyne, which reduces the polarity of the C-H bond and consequently decreases acidity. 2. **Polarity of C-H Bond**: The more polar the C-H bond, the stronger the acid. ### Step 2: Analyze the Given Alkynes Let’s analyze the acidic strength of the alkynes based on the presence of substituents: - **Alkyne A (CH≡CH)**: This alkyne has no substituents. Therefore, it has the highest acidity because there are no electron-donating groups to decrease the polarity of the C-H bond. - **Alkyne B (CH3C≡CH)**: Here, a methyl group (CH3) is attached to one of the carbons of the alkyne. The methyl group is an electron-donating group, which increases the electron density around the carbon and decreases the polarity of the C-H bond. Thus, the acidity is lower than that of alkyne A. - **Alkyne C (CH3C≡CCH3)**: In this case, two methyl groups are attached to the alkyne. The presence of two electron-donating groups further increases the electron density and decreases the polarity of the C-H bond even more than in alkyne B. Therefore, this alkyne has the lowest acidity among the three. ### Step 3: Establish the Trend Based on the analysis: - Alkyne A (CH≡CH) is the most acidic. - Alkyne B (CH3C≡CH) is less acidic than A. - Alkyne C (CH3C≡CCH3) is the least acidic. Thus, the correct trend of acidic nature is: **CH≡CH > CH3C≡CH > CH3C≡CCH3** ### Conclusion The correct order of acidity among the given alkynes is: **Option A: CH≡CH > CH3C≡CH > CH3C≡CCH3** ---
Promotional Banner

Topper's Solved these Questions

  • HYDROCARBONS

    NCERT FINGERTIPS ENGLISH|Exercise Higher Order Thinkin Skills|7 Videos
  • HYDROCARBONS

    NCERT FINGERTIPS ENGLISH|Exercise Assertion & Reason|15 Videos
  • EQUILIBRIUM

    NCERT FINGERTIPS ENGLISH|Exercise Assertion And Reason|15 Videos
  • HYDROGEN

    NCERT FINGERTIPS ENGLISH|Exercise Assertion And Reason|15 Videos

Similar Questions

Explore conceptually related problems

Order of acidic nature

The correct order of acidic strength of the following is

The correct order of acidic strength of the following is

Find the correct order of acid strength of the following acids in aqueous solution

The correct order of increasing basic nature of the following bases is

The correct of acidities of the following is :

The correct order of acid strength of the following compounds:

The correct order of acidity for the following compounds is

The correct order of acidity for the following compounds is

NCERT FINGERTIPS ENGLISH-HYDROCARBONS -Assertion And Reason
  1. The correct trend of acidic nature of the following alkynes is

    Text Solution

    |

  2. Assertion: 2,2-Dimethylbutane does not have any tertiary carbon atom. ...

    Text Solution

    |

  3. Assertion: The reaction, C(2)H(5)Br +2Na+C(2)H(5)Br to C(4)H(10)+2NaBr...

    Text Solution

    |

  4. Assertion: Wurtz reaction is not preferred for the preparation of alka...

    Text Solution

    |

  5. Assertion: Sodium salt of butanoic acid on heating with soda lime give...

    Text Solution

    |

  6. Assertion: Boiling point of pentane is higher than 2,2-dimethylpropane...

    Text Solution

    |

  7. Assertion: Iodination of alkanes is carried out in the presence of oxi...

    Text Solution

    |

  8. Assertion: Staggered conformation of ethane is most stable while eclip...

    Text Solution

    |

  9. Assertion: cis-form of alkene is found to be more polar than the trans...

    Text Solution

    |

  10. Assertion: Alkenes are easily attacked by electrophilic reagents. Re...

    Text Solution

    |

  11. Assertion: Addition of HBr to propene yields 2-bromopropane but in pre...

    Text Solution

    |

  12. Assertion: Decolourisation of KMnO(4) solution is used as a test for u...

    Text Solution

    |

  13. Assertion: Ethyne reacts with sodium metal and sodamide to form sodium...

    Text Solution

    |

  14. Assertion: Cyclopentadienyl anion is aromatic in nature. Reason: Cyc...

    Text Solution

    |

  15. Assertion: The second substituent may enter the mono-substituted benze...

    Text Solution

    |

  16. Assertion: In case of aryl halides, halogens are moderately deactivati...

    Text Solution

    |