Answer:
Q= 245 =2.5 * 10^2
Explanation:
ΔG = ΔGº + RTLnQ, so also ΔGº= - RTLnK
R= 8,314 J/molK, T=298K
ΔGº= - RTLnK = - 6659.3 J/mol = - 6.7 KJ/mol
ΔG = ΔGº + RTLnQ → -20.5KJ/mol = - 6.7 KJ/mol + 2.5KJ/mol* LnQ
→ 5.5 = LnQ → Q= 245 =2.5 * 10^2
Answer:
The pH of 0.1 M BH⁺ClO₄⁻ solution is <u>5.44</u>
Explanation:
Given: The base dissociation constant:
= 1 × 10⁻⁴, Concentration of salt: BH⁺ClO₄⁻ = 0.1 M
Also, water dissociation constant:
= 1 × 10⁻¹⁴
<em><u>The acid dissociation constant </u></em>(
)<em><u> for the weak acid (BH⁺) can be calculated by the equation:</u></em>

<em><u>Now, the acid dissociation reaction for the weak acid (BH⁺) and the initial concentration and concentration at equilibrium is given as:</u></em>
Reaction involved: BH⁺ + H₂O ⇌ B + H₃O+
Initial: 0.1 M x x
Change: -x +x +x
Equilibrium: 0.1 - x x x
<u>The acid dissociation constant: </u>![K_{a} = \frac{\left [B \right ] \left [H_{3}O^{+}\right ]}{\left [BH^{+} \right ]} = \frac{(x)(x)}{(0.1 - x)} = \frac{x^{2}}{0.1 - x}](https://tex.z-dn.net/?f=K_%7Ba%7D%20%3D%20%5Cfrac%7B%5Cleft%20%5BB%20%5Cright%20%5D%20%5Cleft%20%5BH_%7B3%7DO%5E%7B%2B%7D%5Cright%20%5D%7D%7B%5Cleft%20%5BBH%5E%7B%2B%7D%20%5Cright%20%5D%7D%20%3D%20%5Cfrac%7B%28x%29%28x%29%7D%7B%280.1%20-%20x%29%7D%20%3D%20%5Cfrac%7Bx%5E%7B2%7D%7D%7B0.1%20-%20x%7D)





<u>Therefore, the concentration of hydrogen ion: x = 3.6 × 10⁻⁶ M</u>
Now, pH = - ㏒ [H⁺] = - ㏒ (3.6 × 10⁻⁶ M) = 5.44
<u>Therefore, the pH of 0.1 M BH⁺ClO₄⁻ solution is 5.44</u>
The properties of the atomic orbital are actually
dependent on the quantum numbers.
size of atomic orbital: governed by the principal quantum
number (n)
shape of atomic orbital: governed by the angular momentum
quantum number (l)
orientation in space: governed by the magnetic quantum
number (ml)
Since we are asked about the shape, hence the correct answer
is:
angular momentum quantum number (l)
Complete question from other source attached
Answer:
Explanation:
Catalyzed by DNA polymerase - both. DNA polymerase catalyzes DNA replication in the cell. However, purified versions of the enzyme are also used to synthesise DNA as part of PCR reactions
involves leading strand synthesis only - PCR. In PCR, lagging strand synthesis is not carried out because the DNA is denatured (rendered single stranded). Therefore, each strand is replicated independently by leading strand synthesis
duplicates a small fragment of the genome - PCR. Usually, to carry out PCR, small sequences called primers are used that specify the region of DNA to be replicated
duplicates the entire genome - in vivo replication - when the DNA is replicated in vivo, the entire genome is replicated. This is carried out prior to cell division so that two daughter cells can each inherit a copy of the entire genome