1. 3 significant figures
2. 5 significant figures
3. 3 significant figures
4. 4 significant figures
5. 5 significant figures
6. 2 significant figures
7. 4 significant figures
8. 1 significant figure
9. 4 significant figures
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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Answer:
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Answer:
Al³⁺, S²⁻; Al₂S₃
Explanation:
Al is a metal, so it loses its three valence electrons in a reaction to form Al³⁺ ions.
S is a nonmetal. It needs two more electrons to complete its octet, so it tends to form S²⁻ ions.
We can use the criss-cross method to work out the formula of the compound.
The steps are
- Write the symbols of the anion and cation.
- Criss-cross the numbers of the charges to become the subscripts of the other ion.
- Write the formula with the new subscripts.
- Divide the subscripts by their highest common factor.
- Omit all subscripts that are 1.
When we use this method with Al³⁺ and S²⁻, the formula for the compound formed becomes Al₂S₃ .