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.
There is too much light entering her eyes.
Answer:
It slows down the transfer of thermal energy from outside to inside the coat.
Explanation:
2, 4, 1
Explanation:
We have the following chemical reaction:
Ag₂O → Ag + O₂
To balance the chemical equation the number of atoms of each element entering the reaction have to be equal to the number of atoms of each element leaving the reaction, in order to conserve the mass.
So the balanced chemical equation is:
2 Ag₂O → 4 Ag + O₂
Learn more about:
balancing chemical equations
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