The first one will be A. The second one is B.
Here are my reasonable beliefs
For number 1. what the answer seems to be is C.Than looking are numbers two and three their answers are both B
My reasoning for them is , because if you think about the solid liquid gas's this is a common result in most experiments.also for number two , you have to decrease ( go down ) on the concentration ( hardness ) of the subject to get a more powerful solution
So far as number one , for it to be water the atoms have to be far away from the other moving freely , to be a solid they can barely move at all.
Answer: d
Explanation:
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Answer:
Explanation has been given below
Explanation:
- In diaxial conformation of cis-1,3-disubstituted cyclohexane, 4 gauche-butane interactions along with syn-diaxial interaction are present. Hence it readily gets converted to diequitorial conformation where no such gauche-butane interaction is present
- In two possible conformations of trans-1,3-disubstituted cyclohexane, 2 gauche-butane interactions are present in each of them.
- Hence cis-1,3-disubstituted cyclohexane exists almost exclusively in diequitorial form. But trans-1,3-disubstituted cyclohexane has no such option.
- Trans-1,3-disubstituted cyclohexane experiences gauche butane interaction in each of the two conformations.
- Therefore cis-1,3-disubstituted cyclohexane is more stable than trans conformation