Answer:
<h2>The answer you are looking for is (B)</h2>
Explanation:
hope this helps
<h2>please mark as brainliest!!!</h2>
d...................................................
Answer:
The most stable conformer would be the anti-conformer when the substituent methyl groups are farthest away from each other.
Explanation:
Isomers are chemical compounds with the same molecular formula but with different molecular structures.
Conformers are a special type of isomers that produce different structures when the substituents of a Carbon-Carbon single bond (C-C) are rotated.
In 2,3 dimethyl butane, the substituent methyl groups are located around the second and third Carbon to Carbon single bond.
To achieve a stable configuration, the methyl group substituents need to be as far apart as possible (that is, in an anti-position) to minimise repulsion.
The closer the methyl groups are to each other, the more they repel each other and the more unstable the conformer becomes.
That is a capital U with the number 238 at upper left of the letter
Answer:
the answer is a because thermal energy is heat and the question said that is not a factor of thermal energy so A does not refer to heat
