The bond angle about oxygen in alcohols and ethers is typically quite close to tetrahedr...

The bond angle about oxygen in alcohols and ethers is typically quite close to tetrahedral (109.5°), but opens up significantly in response to extreme steric crowding, for example, in going from tert-butyl alcohol to di-tert-butyl ether:

This is entirely consistent with the notion that while lone pairs take up space, they can be “squeezed” to relieve crowding. Another way to relieve unfavorable steric interactions (without changing the position of the lone pairs) is to increase the CO bond distance.

a. Build tert-butyl alcohol and di-tert-butyl ether and optimize the geometry of each using the HF/6-31G* model. Are the calculated bond angles involving oxygen in accord with the values given earlier, in particular with regard to the observed increase in bond angle? Do you see any lengthening of the CO bond in the ether over that in the alcohol? If not, or if the effect is very small (0.01Å), speculate why not.

b. Next, consider the analogous trimethylsilyl compounds Me₃SiOH and Me₃SiOSiMe₃. Calculate their equilibrium geometries using the HF/6-31G* model. Point out any similarities and any differences between the calculated structures of these compounds and their tert-butyl analogues. In particular, do you see any widening of the bond angle involving oxygen in response to increased steric crowding? Do you see lengthening of the SiO bond in the ether over that of the alcohol? If not, rationalize what you do see.