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Question: In which of the following molecules, vacant orbital cannot participate in bonding? A. \[{B_2}{H_6}...

In which of the following molecules, vacant orbital cannot participate in bonding?
A. B2H6{B_2}{H_6}
B. Al2Cl6A{l_2}C{l_6}
C. [H3N. BF3]\left[ {{H_3}N.{\text{ }}B{F_3}} \right]
D. Si2H6S{i_2}{H_6}

Explanation

Solution

Back bonding is the bonding between two atoms in which one atom can have one vacant orbital and the other have a lone pair of electrons.

Complete step by step answer:
Back bonding is a type of resonance. It is the sharing of electrons between the atomic orbital on one atom with the antibonding orbital on another atom.
Back bonding is only possible In [H3N. BF3]\left[ {{H_3}N.{\text{ }}B{F_3}} \right] due to the presence of an empty p-orbital on B and lone pairs of electrons on the p orbital of F. In this case B act as a Lewis acid and F act as a Lewis base. Lone pair on the F is donated to the p orbital of B.
We know that F is highly electronegative in nature. So, it has a tendency to take back the electrons which are donated to B. So there will be a continued jumping of electrons.

Hence the correct answer is (C) i.e [H3N. BF3]\left[ {{H_3}N.{\text{ }}B{F_3}} \right] . Due to back bonding its orbital is not available for bonding.

Note:
Back bonding increases the stability of molecules. This bonding occurs mostly in organometallic compounds. In metal carbonyls the presence of back bonding will decreases the bond order and COC - O bond length will increase. This will decrease the COC - O stretching frequency and increase the MCM - C Bond order. Hence MCM - C bond length decreases and MCM - C stretching frequency increases. Back bonding can affect the properties such as dipole moment, hybridisation etc. CO, N(SiH3)3,PF3N{\left( {Si{H_3}} \right)_{3,}}P{F_3} are some molecules showing back bonding.