Answer:
Carbons 1 and 3
Explanation:
We must remember that by definition <u>alpha carbon</u>s are the carbon (or carbons) next to the carbon that contains the main group. In this case, the main group is the carbonyl group (C = O) in the middle of the molecule. In the acetone molecule, we have three carbons, the carbons neighboring the carbon of the carbonyl group (carbon two) will be the <u>alpha carbons</u>. (Red and blue carbons or carbons one and three)
See figure 1 for further explanations.
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Question: Which solution turns litmus paper blue
Answer: basic
Explanation:compound dissolves in water which cause the solution to become alkaline
question answered by
(jacemorris04)
Potassium dichromate reacts with sulfuric acid to form chromic acid, H₂CrO₄ which is a very strong oxidizing agent. The secondary alcohol, (<em>R</em>)-2-butanol will be oxidized in the presence of chromic acid, but it can only be as oxidized as far as the ketone, which is the product shown, 2-butanone.
Sodium borohydride is a reducing agent that will reduce a ketone or aldehyde to an alcohol. When sodium borohydride reacts with 2-butanone, it reduces it to 2-butanol. However, the alcohol is no longer chiral as it was in the beginning since the sodium borohydride can add a hydride to either face of the carbonyl, which results in a racemic mixture of alcohols. This explains why the product has the same refractive index and boiling point as (<em /><em>R</em>)-2-butanol, however, the product formed would no longer be optically active.
Answer:
0.22 mol / L
Explanation:
Please see the answer in the picture attached below.
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