Replacement of methyl groups of camphor is a reduction mechanism. Camphor is a bridged bi-cyclic compound. If you observe the structure of camphor the methyl group is placed with one carbon bridge (7, 7) and two carbon bridge (1). Attack from face of one carbon bridge is termed as exo attack whereas from face of two carbon bridge is termed as endo attack. So replacement will lead to mix of both and formation of two stereo isomers.
Reduction mechanism is often shown with a U-shaped arrow pointing the attack by ion such as in nucleophilic addition reaction.
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<span>Hey! Dependent variable parameter, I believe is the correct answer. (:</span>
The mineral that you described is called Muscovite. The pages of the book description fits muscovite found in granite pegmatites where it is found in large crystals with a
pseudohexagonal outline that are called "books".
Answer:
A reduction potential measures the tendency of a molecule to be reduced by taking up new electrons. ... Standard reduction potentials can be useful in determining the directionality of a reaction. The reduction potential of a given species can be considered to be the negative of the oxidation potential.
Explanation:
