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Answer:
Explanation:
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In this case, since the undergoing chemical reaction is:
We first need to identify the limiting reactant given the masses of nitrogen and hydrogen:
It means that only 0.647 moles of ammonia are yielded, so the resulting enthalpy change is:
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Between equatorial positions, the F-P-F angle is 120°, and between axial and equatorial positions, it is 90°.
<h3>What in chemical bonding is equatorial position?</h3>
Equatorial Organic Chemistry Illustrated Glossary. Equatorial: In cyclohexane, a bond that runs parallel to the ring's axis (i.e., it follows the chair's equator), or a group joined by such a bond. Positions A are axial, and positions E are equatorial.
<h3>Why do equatorial positions have greater stability?</h3>
As was said in the preceding section, the equilibrium favors the more stable conformer because the chair conformation, in which the methyl group is equatorial, lowers steric repulsion. All monosubstituted cyclohexanes share this property.
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