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Question

The bond angle of C-C bonds in Benzene are _______________.

The correct answer is

All 120°

Bond Angle of C-C Bonds in Benzene Explained

Benzene is a highly stable organic molecule with the chemical formula C$_6$H$_6$. It has a unique structure consisting of a six-membered ring of carbon atoms, with one hydrogen atom attached to each carbon atom.

Let's understand the structure and bonding in Benzene to determine the C-C bond angles:

  • Benzene has a planar, hexagonal structure.
  • Each carbon atom in the Benzene ring is bonded to two other carbon atoms and one hydrogen atom.
  • Due to resonance, the bonds between carbon atoms are neither pure single nor pure double bonds; they are intermediate in character, often depicted as a ring inside the hexagon.
  • Each carbon atom in Benzene is sp$^2$ hybridized.
  • sp$^2$ hybridization leads to a trigonal planar geometry around the central atom, with ideal bond angles of 120°.

In the Benzene ring, the carbon atoms form C-C-C bonds. Since each carbon atom is sp$^2$ hybridized and the structure is a regular hexagon, the bond angle between any two adjacent C-C bonds (i.e., the C-C-C angle) is determined by the geometry of the sp$^2$ hybridized carbon atom within the hexagonal ring.

For a perfect hexagon, the internal angle is 120°. Since Benzene is a planar hexagon with sp$^2$ hybridized carbons, all the C-C-C bond angles are 120°.

Therefore, the bond angle of C-C bonds in Benzene (referring to the angle between adjacent C-C bonds, i.e., the C-C-C angle) is 120° for all such angles in the ring.

Let's consider the given options:

  • All 120°: This aligns with the structural analysis of Benzene.
  • Three are 180° and three are 120°: 180° implies a linear geometry, which is not present in the cyclic Benzene structure.
  • All are 60°: A 60° angle in a six-membered ring would introduce significant ring strain (like in cyclopropane, which has 60° bond angles and is highly strained). Benzene is known for its stability and absence of significant ring strain.
  • Three are 60° and three are 120°: This mix does not fit the symmetrical, regular hexagonal structure of Benzene.

Based on the sp$^2$ hybridization and the planar hexagonal geometry of Benzene, all the C-C-C bond angles are 120°.

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Important Questions from Haloalkanes And Haloarenes

  1. IUPAC name of neopentyl chloride is

  2. Among the following statements, choose the correct statements.

    A. SN2 reaction proceeds with stereo chemical inversion.

    B. The process of conversion of Racemic mixture into enantiomer is known as Racemisation

    C. A mixture containing 2 enantiomers in equal proportions is known as Racemic mixture.

    D. The stereoisomers related to each other as superimposable mirror image are called enantiomers.

    E. The objects which are non- superimposable on their mirror image are said to be chiral and this properly is known as chirality.

    Choose the correct answer from the options given below:

  3. Which of the following would yield a single monohalogen derivative?

  4. The index of hydrogen deficiency (IHD) of benzene is

  5. The given hydrocarbon is CH3 - CH2 - CH2 - CH2 - CH3

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