Answer:
Axial position
Explanation:
In the reduction of 4-tert-butylcyclohexanone with sodium borohydride, the major product has the tert-butyl group in the equatorial position and the alcohol in the axial position.
The reason for this is that, axial bonds are parallel to each other. If substituents are larger than hydrogen, they experience a greater steric crowding in axial compared to the equatorial position. Therefore, many substituted cyclohexane compounds prefer a conformation in which the larger substituents are in equatorial position.
Answer:
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Answer:
A catalyst speeds up a chemical reaction, without being consumed by the reaction. It increases the reaction rate by lowering the activation energy for a reaction. ... Remember that with a catalyst, the average kinetic energy of the molecules remains the same but the required energy decreases
Explanation:
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Answer:
This would be the hydride ion where H gains an electron from a metal such as Na
Explanation:
Answer:
Glossopteris
Explanation:
Glossopteris is a fossil fern that helped support Wegener's hypothesis.
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