Answer:
Twice as much.
Explanation:
That's because the freezing point depression depends on the total number of solute particles.
C₆H₁₂O₆(s) ⟶ C₆H₁₂O₆(aq)
0.01 mol of C₆H₁₂O₆ gives 0.01 mol of solute particles.
NaCl(s) ⟶ Na⁺(aq) + Cl⁻(aq)
1 mol of NaCl gives 0.01 mol of Na⁺(aq) and 0.01 mol of Cl⁻(aq).
That's 0.02 mol of particles, so the freezing point depression of 0.01 mol·L⁻¹ NaCl will be twice that of 0.01 mol·L⁻¹ C₆H₁₂O₆.
A bee a bike a water fall
The answer is c. the others are compounds.
M(NaCl)=50.0 g
m(H₂O)=150.0 g
m(solution)=m(NaCl)+m(H₂O)
w(NaCl)=100m(NaCl)/m(solution)=100m(NaCl)/{m(NaCl)+m(H₂O)}
w(NaCl)=100*50.0/(50.0+150.0)=25%
Answer:
Here's what I get.
Explanation:
The MO diagrams of KrBr, XeCl, and XeBr are shown below.
They are similar, except for the numbering of the valence shell orbitals.
Also, I have drawn the s and p orbitals at the same energy levels for both atoms in the compounds. That is obviously not the case.
However, the MO diagrams are approximately correct.
The ground state electron configuration of KrF is

KrF⁺ will have one less electron than KrF.
You remove the antibonding electron from the highest energy orbital, so the bond order increases.
The KrF bond will be stronger.