The more adjacent C-H bonds are the larger hyperconjugation stabilization is.

The C-H bonds of fats are much less polar.

Both theoretical studies as well as experiments now show that C-H bonds can be broken.

The other six C-H bonds lie almost parallel to the mean plane, and are said to be equatorial.

The four C-H bonds are equal because they resonate.

They are usually more chemically reactive than aliphatic C-H bonds.

Methane is a tetrahedral molecule with four equivalent C-H bonds.

All three enzymes activate a C-H bond adjacent to a carbonyl group.

Such radiation breaks the C-H bonds and significantly reduces the luminescence yield.

The first step in the catalytic cycle is cleavage of the allylic C-H bond.