Answer:
yes, if they were in rest they would have potential energy
Explanation:
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.
I don’t understand your language sorry
Answer:
Let x equal the percentage abundance of one of the two isotopes. The other isotope must then have an abundance of 100 percent minus x percent, which you express in decimal form as (1 - x). For nitrogen, you can set x equal to the abundance of N14 and (1 - x) as the abundance of N15.
Explanation:
The answer is C I Juss did it
Brainliestttt please
Is c bc the xy2 is the correct one
