<span><span>Dipole-dipole interactions , example: ammoni </span><span>forces, example: methane, CH4</span><span>Hydrogen bonding example: water, H2O </span></span>
Answer:
Axial
Explanation:
In the most stable conformation of Cis-3-tert-Butylcyclohexanol, the tert-butyl group is at equatorial position and the alcohol group is in the axial position.
If the tert-butyl group is placed in equatorial position, repulsions are minimized. The bulkier the group, the greater the energy difference between the axial and equatorial conformers. Hence for a ring having a bulky substituent, such bulky substituent is better placed in the equatorial position.
The energy difference between the conformers of Cis-3-tert-Butylcyclohexanol is so high that the compound is almost "frozen" in a conformation where the tert-butyl groups are equatorial and the -OH groups are axial. This conformer is more stable by 24 KJ/mol.
Explanation:
A chemical reaction is defined as the reaction in which bonds between the reactants either break or form which leads to the formation of a new substance.
For example, 
So, when we drop a sodium metal into water then it produces a frizzing sound which shows the metal is reacting with water.
We know that when two aqueous solutions chemically react with each other then it may lead to the formation of an insoluble substance which is known as precipitate.
This means that formation of a precipitate is also a chemical reaction.
Thus, we can conclude that following are the statements which show evidence for a chemical reaction.
- Dropping sodium metal into water produces fizzing.
- Mixing two aqueous solutions produces a precipitate.