Home
Class 12
CHEMISTRY
Which of the following is optically acti...

Which of the following is optically active?

A

Ethylene glycol

B

Oxalic acid

C

Glycerol

D

Tartaric acid

Text Solution

AI Generated Solution

The correct Answer is:
To determine which of the given compounds is optically active, we need to identify if they contain any chiral centers. A chiral center is typically a carbon atom that is bonded to four different groups. Let's analyze each option step-by-step. ### Step 1: Analyze Ethylene Glycol - **Structure**: Ethylene glycol has the formula \( \text{HO-CH}_2-\text{CH}_2-\text{OH} \). - **Chirality Check**: - The first carbon is attached to two hydrogen atoms and one hydroxyl group (OH) and one carbon atom. - The second carbon is similarly attached to two hydrogen atoms and one hydroxyl group and one carbon atom. - **Conclusion**: Both carbons are not chiral because they are not attached to four different groups. - **Result**: Ethylene glycol is **not optically active**. ### Step 2: Analyze Oxalic Acid - **Structure**: Oxalic acid has the formula \( \text{HOOC-COOH} \). - **Chirality Check**: - The carbon atoms are each bonded to two oxygen atoms (due to the double bonds) and one hydroxyl group. - **Conclusion**: Neither carbon is chiral as they do not have four different substituents. - **Result**: Oxalic acid is **not optically active**. ### Step 3: Analyze Glycerol - **Structure**: Glycerol has the formula \( \text{HO-CH}_2-\text{CHOH}-\text{CH}_2-\text{OH} \). - **Chirality Check**: - The first carbon is attached to two hydrogen atoms and one hydroxyl group. - The second carbon is attached to one hydroxyl group and two hydrogen atoms. - The third carbon is also attached to two hydrogen atoms and one hydroxyl group. - **Conclusion**: None of the carbons are chiral as they do not have four different groups. - **Result**: Glycerol is **not optically active**. ### Step 4: Analyze Tartaric Acid - **Structure**: Tartaric acid has the formula \( \text{HOOC-CHOH-CHOH-COOH} \). - **Chirality Check**: - The first carbon (attached to COOH) is bonded to four different groups: COOH, OH, H, and the rest of the molecule. - The second carbon (attached to OH) is also bonded to four different groups: COOH, OH, H, and the rest of the molecule. - **Conclusion**: Both of these carbons are chiral. - **Result**: Tartaric acid is **optically active**. ### Final Answer The compound that is optically active is **Tartaric Acid**. ---
Promotional Banner

Topper's Solved these Questions

  • ALDEHYDES, KETONES AND CARBOXYLIC ACIDS

    AAKASH INSTITUTE ENGLISH|Exercise Assignment (SECTION -B OBJECTIVE TYPES QUESTIONS (ONE OPTION IS CORRECT)|24 Videos
  • ALDEHYDES, KETONES AND CARBOXYLIC ACIDS

    AAKASH INSTITUTE ENGLISH|Exercise Assignment (SECTION -C Objective type questions more than one options are correct)|11 Videos
  • ALDEHYDES, KETONES AND CARBOXYLIC ACIDS

    AAKASH INSTITUTE ENGLISH|Exercise Illustrations|3 Videos
  • ALCOHOLS, PHENOLS AND ETHERS

    AAKASH INSTITUTE ENGLISH|Exercise Try Yourself|5 Videos
  • AMINES

    AAKASH INSTITUTE ENGLISH|Exercise Assignment Section -J (Aakash Challengers Questions)|9 Videos

Similar Questions

Explore conceptually related problems

Which of the following is optically inactive ?

Which of the following be optically active ?

Which of the following is optical active subtance ?

Which of the following is/are optically active?

Which of the following is not optically active?

Which of the following is not optically active?

Which of the following is an optically inactive compound?

Which of the following shows optical activity?

AAKASH INSTITUTE ENGLISH-ALDEHYDES, KETONES AND CARBOXYLIC ACIDS -Assignment (Section A Competition Level Questions)
  1. The reaction of acetaldehyde with HCN followed by hydrolysis gives a p...

    Text Solution

    |

  2. Which factors will increase the reactivity of group? (i) Presence of...

    Text Solution

    |

  3. Which of the following is optically active?

    Text Solution

    |

  4. identify the wrong statement from the following:

    Text Solution

    |

  5. The general formula of C(n)H(2n)O(2) could be for open chain

    Text Solution

    |

  6. The IUPAC name of the phthalic acid-

    Text Solution

    |

  7. In the following reaction, product (P ) is R-overset(O)overset("||")...

    Text Solution

    |

  8. Dry distillation of calcium acetate gives :

    Text Solution

    |

  9. CH(3)-CH(2)-C -=CH overset( R)underset(H(3)O^(oplus))to Butanone, R is

    Text Solution

    |

  10. Which of the following pathways produces 2-hexanone? (i) 1-Hexyne is...

    Text Solution

    |

  11. An alkene of molecular formula C(9) H(18) on ozonolysis gives 2.2 dime...

    Text Solution

    |

  12. (CH(3))(2)COoverset(NaCN)underset(HCI)rarr(A)underset(Delta)overset(H(...

    Text Solution

    |

  13. A liquid was mixed with ethanol and a drop of concentrated H(2) SO(4) ...

    Text Solution

    |

  14. The major product obtained on interaction of phenol with sodium hydrox...

    Text Solution

    |

  15. Which of the following does not give benzoic acid on hydrolysis?

    Text Solution

    |

  16. The compound x is

    Text Solution

    |

  17. Acetic acid is obtained when

    Text Solution

    |

  18. When m-chlorobenzaldehyde is treated with 50% KOH solution, the produc...

    Text Solution

    |

  19. Aldol condensation will not be observed in

    Text Solution

    |

  20. Whch of the following gives aldol condensation reaction?

    Text Solution

    |