1) <u>Stereo-selective (or enantioselective)</u> reactions form predominately or exclusively one enantiomer.
2) Epoxidation is the addition of a single oxygen atom to an alkene to form an epoxide.
3) <u>Hydrogenation (or reduction)</u> of an alkene forms an alkane by addition of H₂.
4) <u>Dihydroxylation</u> is the addition of two hydroxy groups to a double forming, a 1,2-diol or glycol.
5) <u>oxidative</u> cleavage of an alkene breaks both the σ and π bonds of the double bond to form two carbonyl groups.
6) <u>Regioselective</u> reactions form predominately or exclusively one constitutional isomer.
7) <u>Syn</u> dihydroxylation results when an alkene is treated KMnO4 or OsO4, where each reagent adds two oxygen atoms to the same side of the double bond.
Answer:
A lot of them.
Explanation:
It would take hundreds of thousands of trees to clear all of the emmisions.
Answer is: hydrogen bonding.
Methanol has stronger intermolecular bonds than methane.
Intermolecular forces are the forces between molecules or particles.
There are several types of intermolecular forces: hydrogen bonding, ion-induced dipole forces, ion-dipole forces andvan der Waals forces.
Hydrogen bond is an electrostatic attraction between two polar groups that occurs when a hydrogen atom (H), covalently bound to a highly electronegative atom such as flourine (F), oxygen (O) and nitrogen (N) atoms.
Answer:
No, Mercury can actually cause poisoning. That is why other metals, such as Alkaline metals, are used in making batteries
