If I remember correctly, you would have to heat the reaction beaker over a burner..
I apologize if I'm wrong
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.
Ionic bonds are a metal and a non metal bond and a covalent bond is two no metals banded together.
Answer:
Explanation:
Hello there!
In this case, since we have a problem about volume-pressure relationship, the idea here is to use the Boyle's law to calculate the final volume as shown below:
Then, we plug in the initial and final pressures and the initial volume to obtain:
Regards!
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