Home
Class 12
CHEMISTRY
CH(3)CHO is more reactive than CH3COCH3 ...

`CH_(3)CHO` is more reactive than `CH_3COCH_3` towards reaction with HCN. Give reason.

Text Solution

AI Generated Solution

To understand why CH₃CHO (acetaldehyde) is more reactive than CH₃COCH₃ (acetone) towards reaction with HCN (hydrogen cyanide), we need to analyze the structures and the electronic effects present in these compounds. ### Step-by-Step Solution: 1. **Identify the Structures**: - CH₃CHO is acetaldehyde, which has the structure: ``` O ...
Promotional Banner

Topper's Solved these Questions

  • ALDEHYDES,KETONES AND CARBOXYLIC ACIDS

    CBSE COMPLEMENTARY MATERIAL|Exercise SHORT ANSWER -I TYPE QUESTIONS (2 MARKS)|30 Videos
  • ALDEHYDES,KETONES AND CARBOXYLIC ACIDS

    CBSE COMPLEMENTARY MATERIAL|Exercise SHORT ANSWER -II TYPE QUESTIONS (3 MARKS)|44 Videos
  • ALDEHYDES,KETONES AND CARBOXYLIC ACIDS

    CBSE COMPLEMENTARY MATERIAL|Exercise LONG ANSWER TYPE QUESTIONS (5 MARKS)|21 Videos
  • ALCOHOLS, PHENOLS AND ETHERS

    CBSE COMPLEMENTARY MATERIAL|Exercise LONG ANSWER TYPE QUESTIONS (5 Marks)|5 Videos
  • AMINES

    CBSE COMPLEMENTARY MATERIAL|Exercise 5 MARKS|7 Videos

Similar Questions

Explore conceptually related problems

Give the mechanism of cyanohydrin formation when carbonyl compounds react with HCN in the presence of alkali. (b) Why CH_(3)CHO is more reactive than CH_(3)COCH_(3) towards reaction with HCN ?

Account for the following : (i) CH_(3)CHO is more reactive than CH_(3)COCH towards reaction with HCN . (ii) Carboxylic acid is a stronger acid then phenol . (b) Wrtie the chemical equations to illuustrate the following reaction : (i) Wolff-Kishner reduction (ii) Aldol condensation (iii) Cannizzaro reaction

CH_(3)CH_(2)I is more reactive than CH_(3)CH_(2)Cl towards KCN.

CH_(3)CH_(2)I is more reactive than CH_(3)CH_(2)Cl towards KCN.

(a) Give reasons : (i) CH_(3)-CHO is more reactive than CH_(3)COCH_(3) towards HCN. (ii) 4-nitrobenzoic acid is more acidic than benzoic acid. (b) Describe the following : (i) Acetylation (ii) Cannizzaro reaction. (iii) Cross aldol condensation.

CH_(3)CH=CHCl is more/less reactive than CICH_(2)CH=CH_(2)? .

Statement :I: CH_(3)CHO is more reactive then CH_(3)COCH_(3) :Statement II; The C=0 group in CH_(3)CHO experiences more steric hidderance

CBSE COMPLEMENTARY MATERIAL-ALDEHYDES,KETONES AND CARBOXYLIC ACIDS-VERY SHORT ANSWER TYPE QUESTIONS (1 MARK)
  1. Arrange the following compounds in an increasing order of their acid s...

    Text Solution

    |

  2. Draw the structure of he compound whose IUPAC name is 4-chloropentan2-...

    Text Solution

    |

  3. Which type of aldehyde can go Cannizzaro reaction ?

    Text Solution

    |

  4. Name the aldehyde which does not give Fehling's solution test.

    Text Solution

    |

  5. Arrange the following in the order of their incresing reactivity towar...

    Text Solution

    |

  6. Mention industrial product obtained from HCHO.

    Text Solution

    |

  7. Arrange the following compounds in increasing order of their boiling p...

    Text Solution

    |

  8. How is acetone obtained from ethanol ?

    Text Solution

    |

  9. Why do aldehydes and ketones have lower boiling point than alcohols ?

    Text Solution

    |

  10. Write reaction between acetyl chloride and dimethyl cadmium.

    Text Solution

    |

  11. What happens when CH(3)CHO is treated with K(2)Cr(2)O(7) in presence o...

    Text Solution

    |

  12. Write the IUPAC name of .

    Text Solution

    |

  13. Give balanced equation and name of products when CH(3)COOH is treated ...

    Text Solution

    |

  14. What product is obtained when ethyl benzene is oxidized with alkaline ...

    Text Solution

    |

  15. CH(3)CHO is more reactive than CH3COCH3 towards reaction with HCN. Giv...

    Text Solution

    |

  16. What is RDX ?

    Text Solution

    |

  17. HOOC-CH=CH-COOH

    Text Solution

    |

  18. Write the IUPAC name of .

    Text Solution

    |

  19. Why does benzoic acid not undergo Friedel-Craft reaction ?

    Text Solution

    |