Answer:
See explanation and image attached
Explanation:
The reaction of 1-bromo-2-tert-butylcyclohexane with potassium tert-butoxide is an elimination reaction that occurs by E2 mechanism.
The E2 reaction proceeds faster when the hydrogens are in an antiperiplanar position at an angle of 180 degrees.
This is only attainable in the trans isomer of 1-bromo-2-tert-butylcyclohexane. Hence trans 1-bromo-2-tert-butylcyclohexane reacts faster with potassium tert-butoxide
1,2-methylcyclohexane, 1,3-methylcyclohexane, 1,4-methylcyclohexane
Answer:
the stabilization of the negative charge in orbitals with higher s character
Explanation:
Acetylide anion is a carbon anion compound or popularly called carbanion. Now Acetylide anion is sp hybridized. However acetylide anion tends to be more acidic as we move from sp³ to sp, hence acidicity increases, which makes sp to have the highest acidity and become the most stable.
So, we can conclude that the acetylide anion is more acidic due to the stabilization of the negative charge in orbitals with higher s character and as the s character increases, acidic nature of acetylide anion also increases.
Answer:
Hyperkalemia
Explanation:
The condition of acidosis can also cause Hyperkalemia because the higher H concentration diffuses to the ICF, pushing K towards the ECF.
