Home
Class 12
CHEMISTRY
An alkene give two moles of HCHO, one mo...

An alkene give two moles of `HCHO`, one mole of `CO_(2)` and one mole of `CH_(3)-underset(O)underset(||)(C )-CHO` on ozonolysis. What is its structure ?

A

`CH_(2)=CH-underset(CH_(3))underset(||)(CH)-CH=CH_(2)`

B

`CH_(2)=C=CH-underset(CH_(2))underset(||)(C )-CH_(3)`

C

`CH_(2)-underset(CH_(3))underset(|)(C)=CH-CH=CH_(2)`

D

`CH_(2)=C=CH-underset(CH_(3))underset(|)(CH)-CH=CH_(2)`

Text Solution

AI Generated Solution

The correct Answer is:
To determine the structure of the alkene that gives two moles of HCHO, one mole of CO2, and one mole of CH3C(=O)CHO upon ozonolysis, we can follow these steps: ### Step 1: Understand the Products of Ozonolysis Ozonolysis of alkenes typically results in the cleavage of double bonds, leading to the formation of carbonyl compounds (aldehydes or ketones). In this case, we have: - 2 moles of HCHO (formaldehyde) - 1 mole of CO2 (carbon dioxide) - 1 mole of CH3C(=O)CHO (which is an aldehyde) ### Step 2: Analyze the Given Products From the products, we can infer: - The presence of two moles of HCHO suggests that two carbon atoms are being oxidized to form formaldehyde. - The formation of CO2 indicates that one of the carbon atoms in the alkene is completely oxidized, losing a carbon atom in the process. - The CH3C(=O)CHO indicates that there is a carbon chain with a carbonyl group (C=O) and an aldehyde group (CHO). ### Step 3: Propose a Structure for the Alkene Given the products, we can propose a structure for the alkene that can yield these products upon ozonolysis. A suitable candidate would be 2-pentene (CH3-CH=CH-CH2-CH3). ### Step 4: Perform Ozonolysis on the Proposed Structure 1. **Ozonolysis of 2-pentene**: - The double bond between the second and third carbon atoms breaks. - The resulting fragments would be: - CH3C(=O)CHO (from the left side of the double bond) - HCHO (from the right side of the double bond) - CO2 (from the carbon that is oxidized completely) ### Step 5: Confirm the Products - From the ozonolysis of 2-pentene, we get: - 1 mole of CH3C(=O)CHO (which corresponds to the aldehyde) - 2 moles of HCHO (from the two terminal carbons) - 1 mole of CO2 (from the carbon that is oxidized) ### Conclusion The structure of the alkene is **2-pentene** (CH3-CH=CH-CH2-CH3). ---

To determine the structure of the alkene that gives two moles of HCHO, one mole of CO2, and one mole of CH3C(=O)CHO upon ozonolysis, we can follow these steps: ### Step 1: Understand the Products of Ozonolysis Ozonolysis of alkenes typically results in the cleavage of double bonds, leading to the formation of carbonyl compounds (aldehydes or ketones). In this case, we have: - 2 moles of HCHO (formaldehyde) - 1 mole of CO2 (carbon dioxide) - 1 mole of CH3C(=O)CHO (which is an aldehyde) ...
Promotional Banner

Topper's Solved these Questions

  • STRUCTURAL IDENTIFICATION

    RESONANCE ENGLISH|Exercise Exercise - 2 (Part-I)|10 Videos
  • STRUCTURAL IDENTIFICATION

    RESONANCE ENGLISH|Exercise Exercise - 2 (Part-II)|8 Videos
  • STRUCTURAL IDENTIFICATION

    RESONANCE ENGLISH|Exercise Exercise-1 (Part-I)|23 Videos
  • STEREOISOMERISM

    RESONANCE ENGLISH|Exercise EXERCISE (PART III : PRACTICE TEST-2 (IIT-JEE (ADVANCED PATTERN))|23 Videos
  • SURFACE CHEMISTRY

    RESONANCE ENGLISH|Exercise Section - 5|1 Videos

Similar Questions

Explore conceptually related problems

One mole of CO_(2) contains:

Which alkene on ozonolysis gives CH_(3)CH_(2)CHO and CH_(3)underset(O)underset(||)(C )CH_(3) ?

Which alkene on ozonolysis gives CH_(3)CH_(2)CHO and CH_(3)underset(O)underset(||)(C )CH_(3) ?

CH_(3)-underset(CH_(2))underset(||)(C )-CH_(2)OH ii CH_(3)-CH=CH-CHO

IUPAC name of CH_(3)-underset(CH_(3))underset(|)C=CH-underset(O)underset(||)C-CH_(3) is

Choose the correct IUPAC name for CH_(3)-underset(CH_(2)-CH_(3))underset(|)(CH)-CHO is -

IUPAC name of CH_(3)-underset(Cl)underset(|)(C)=CH-CH_(2)-underset(O)underset(||)(C)-CH_(3) is

Give IUPAC names of the following: CH_( 2)=underset(CH_(3))underset(CH_(2))underset(|)C-COOH

RESONANCE ENGLISH-STRUCTURAL IDENTIFICATION-Exercise-1 (Part-II)
  1. Which of the following compound will give four monochloro (structural)...

    Text Solution

    |

  2. X overset(O(3)//Zn)rarr , The IUPAC name of compound Y is :

    Text Solution

    |

  3. An alkene give two moles of HCHO, one mole of CO(2) and one mole of CH...

    Text Solution

    |

  4. An unknown compound on ozonolysis to give acid C(3)H(6)O(2) and a keto...

    Text Solution

    |

  5. When one mole of the given compond reacts with sodium metal then how m...

    Text Solution

    |

  6. Compound X is

    Text Solution

    |

  7. , Identify X:

    Text Solution

    |

  8. Lesch Nyhan disease is an X-linked recessive disorder that causes neur...

    Text Solution

    |

  9. Which will undergo reaction with ammonical AgNO(3) :

    Text Solution

    |

  10. Which of the following compounds gives red ppt with Cu(2)Cl(2)//NH(4)O...

    Text Solution

    |

  11. Identify the hydrocarbon having molecular formula C(5)H(6) which gives...

    Text Solution

    |

  12. The group reagent for the test of alcohols is :

    Text Solution

    |

  13. The following two compounds I and II can be distinguished by using rea...

    Text Solution

    |

  14. Which of the following compound will not react with l(2)//OH^(-).

    Text Solution

    |

  15. A compound A gives following reactions. Its structure can be

    Text Solution

    |

  16. An organic compound X (C(4)H(8)O(2)) gives positive test with NaOH an...

    Text Solution

    |

  17. Which of the following compound will give smell of NH(3) with conc. Na...

    Text Solution

    |

  18. Which of the following will not give positive test with CHCl(3)//KOH.

    Text Solution

    |

  19. A positive carbylamine test is shown by :

    Text Solution

    |

  20. The Hinsberg's method is used for :

    Text Solution

    |