Answer:
option a and c both are correct
Explanation:
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Answer:
The reference point is the ground.
Explanation:
•Moves slow that you don't notice hope this helps you :) god loves you :)
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:
0 kcal/mole
Explanation:
The most stable Newman projection corresponds to the minimum potential energy: Answer (e) 0 kcal/mole
