Draw a chair conformation for cis-1-bromo-2,4-dimethylcyclohexane showing equatorial and axial positions at the carbon atoms bea
ring the substituents (all substituents are at cis configuration) g
1 answer:
Answer:
See attachment.
Explanation:
Mono-substituted cyclohexanes are more stable with their substituents in an equatorial position. However, with poly-substituted cyclohexanes, the situation is more complex since the steric effects of all substituents have to be taken into account. In this case, you can see that <u>the interconversion is shifted towards the conformation in the bottom because there is less tension between the substituents</u>.
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Answer:
a. The second run will be faster.
d. The second run has twice the surface area.
Explanation:
The rate of a reaction is proportional to the surface area of a catalyst. Given the volume (V) of a sphere, we can find its surface area (A) using the following expression.
The area of the 10.0 cm³-sphere is:
The area of each 1.25 cm³-sphere is:
The total area of the 8 1.25cm³-spheres is 8 × 5.61 cm² = 44.9 cm²
The ratio of 8 1.25cm³-sphere to 10.0 cm³-sphere is 44.9 cm²/22.4 cm² = 2.00
Since the surface area is doubled, the second run will be faster.