If the vibrational frequency is `omega_(0)` the excitation energy of the first vibrational level will be ` ħ omega_(0)`. Thus if there are `J` ratational levels contained in the band between the ground state and the first vibrational excitation, then
` ħ omega_(0)=(J(J+1) ħ^(2))/(2I)`
where as stated in the problem we have ignored any coupling between the two. For `HF` molecule
`I=(m_(H)m_(F))/(m_(H)+m_(F))d^(2)= 1.336xx10^(-4) gm cm^(2)`
Then `J(J+1)=(2I omega_(0))/( ħ)= 197.4`
For `J=14, J(J+1)= 210`. For `J= 13,J(J+1_= 182`. Thus there lie `13` levels between the ground state and the first vibrational excitation.