Answer:
b) +2 and +3.
Explanation:
Hello,
In this case, given the molecular formulas:

And:

We can relate the subscripts with the oxidation states by knowing that they are crossed when the compound is formed, for that reason, we notice that oxygen oxidation state should be -2 for both cases and the oxidation state of X in the first formula must be +2 since both X and O has one as their subscript as they were simplified:

Moreover, for the second case the oxidation state of X should be +3 in order to obtain 3 as the subscript of oxygen:

Thus, answer is b)+2 and +3
Best regards.
Answer:

Explanation:
Hello,
In this case, since calcium hydroxide a strong base, its dissociation will completely result in both calcium and hydroxyl ions:

Thus, the concentration of hydroxyl ions equals that of the calcium hydroxide, with which we could compute the pOH as shown below:
![pOH=-log([OH^-]}=-log(0.0012)\\\\pOH=2.92](https://tex.z-dn.net/?f=pOH%3D-log%28%5BOH%5E-%5D%7D%3D-log%280.0012%29%5C%5C%5C%5CpOH%3D2.92)
Now, the pH and the pOH are related by:

Hence, the pH finally results:

Best regards.
Answer:
pHe = 3.2 × 10⁻³ atm
pNe = 2.5 × 10⁻³ atm
P = 5.7 × 10⁻³ atm
Explanation:
Given data
Volume = 1.00 L
Temperature = 25°C + 273 = 298 K
mHe = 0.52 mg = 0.52 × 10⁻³ g
mNe = 2.05 mg = 2.05 × 10⁻³ g
The molar mass of He is 4.00 g/mol. The moles of He are:
0.52 × 10⁻³ g × (1 mol / 4.00 g) = 1.3 × 10⁻⁴ mol
We can find the partial pressure of He using the ideal gas equation.
P × V = n × R × T
P × 1.00 L = 1.3 × 10⁻⁴ mol × (0.082 atm.L/mol.K) × 298 K
P = 3.2 × 10⁻³ atm
The molar mass of Ne is 20.18 g/mol. The moles of Ne are:
2.05 × 10⁻³ g × (1 mol / 20.18 g) = 1.02 × 10⁻⁴ mol
We can find the partial pressure of Ne using the ideal gas equation.
P × V = n × R × T
P × 1.00 L = 1.02 × 10⁻⁴ mol × (0.082 atm.L/mol.K) × 298 K
P = 2.5 × 10⁻³ atm
The total pressure is the sum of the partial pressures.
P = 3.2 × 10⁻³ atm + 2.5 × 10⁻³ atm = 5.7 × 10⁻³ atm
Answer:
a) The structure of anthracene is planar with all the pi electrons delocalized in the structure to maintain aromaticity.
b) The C-C bond length in anthracene is about 140 pm with all the bond lengths being similar to each other.
The standard C-C bond length is 154 pm while standard C=C bond is about 134 pm. Therefore the bond length in anthracene is smaller than standard C-C bond length and longer than standard C=C bond length. This can be explained from the fact that the C-C bonds in anthracene has be mixed characteristics of single and double bond because of the delocalization of pi electrons over the whole structure. As a result, they are neither fully single nor fully double bond in nature. Hence the observed bond lengths.
c) This molecule is not flat. The N-atom is sp3 hybridized here and the H-atom attached to N will remain out of plane.
Explanation: