Because they are different elements have different number of protons and neutrons........ I guessed do not trust me...
Answer: only the VSEPR mode shows the geometric shape of a formula.
K(+1)
Mn(x)
O(-2)
1+x-2*4=0
x=7
Answer:
1. The pH of 1.0 M trimethyl ammonium (pH = 1.01) is lower than the pH of 0.1 M phenol (5.00).
2. The difference in pH values is 4.95.
Explanation:
1. The pH of a compound can be found using the following equation:
![pH = -log([H_{3}O^{+}])](https://tex.z-dn.net/?f=%20pH%20%3D%20-log%28%5BH_%7B3%7DO%5E%7B%2B%7D%5D%29%20)
First, we need to find [H₃O⁺] for trimethyl ammonium and for phenol.
<u>Trimethyl ammonium</u>:
We can calculate [H₃O⁺] using the Ka as follows:
(CH₃)₃NH⁺ + H₂O → (CH₃)₃N + H₃O⁺
1.0 - x x x
![Ka = \frac{[(CH_{3})_{3}N][H_{3}O^{+}]}{[(CH_{3})_{3}NH^{+}]}](https://tex.z-dn.net/?f=Ka%20%3D%20%5Cfrac%7B%5B%28CH_%7B3%7D%29_%7B3%7DN%5D%5BH_%7B3%7DO%5E%7B%2B%7D%5D%7D%7B%5B%28CH_%7B3%7D%29_%7B3%7DNH%5E%7B%2B%7D%5D%7D)

By solving the above equation for x we have:
x = 0.097 = [H₃O⁺]
<u>Phenol</u>:
C₆H₅OH + H₂O → C₆H₅O⁻ + H₃O⁺
1.0 - x x x
![Ka = \frac{[C_{6}H_{5}O^{-}][H_{3}O^{+}]}{[C_{6}H_{5}OH]}](https://tex.z-dn.net/?f=Ka%20%3D%20%5Cfrac%7B%5BC_%7B6%7DH_%7B5%7DO%5E%7B-%7D%5D%5BH_%7B3%7DO%5E%7B%2B%7D%5D%7D%7B%5BC_%7B6%7DH_%7B5%7DOH%5D%7D)


Solving the above equation for x we have:
x = 9.96x10⁻⁶ = [H₃O⁺]
![pH = -log([H_{3}O^{+}]) = -log(9.99 \cdot 10^{-6}) = 5.00](https://tex.z-dn.net/?f=%20pH%20%3D%20-log%28%5BH_%7B3%7DO%5E%7B%2B%7D%5D%29%20%3D%20-log%289.99%20%5Ccdot%2010%5E%7B-6%7D%29%20%3D%205.00%20)
Hence, the pH of 1.0 M trimethyl ammonium is lower than the pH of 0.1 M phenol.
2. The difference in pH values for the two acids is:
Therefore, the difference in pH values is 4.95.
I hope it helps you!
Answer:
The compound a is 1-methyl cyclohexene (see attachment for structure).
Explanation:
The reaction of 1-Bromo-1-methylcyclohexane with sodium methoxide is a <u>second-order reaction</u> since the <u>methoxide ion is a strong base</u> and also a strong nucleophile. This ion attacks the alkyl halide faster than the alkyl halide can ionize to produce a first-order reaction. However, we can not see the product of nucleophilic substitution. The SN₂ mechanism is blocked due to the <u>impediment of the 1-Bromo-1-methylcyclohexane</u>. The main product, according to the Zaitsev rule, is the 1-methyl cyclohexene, thus forming a <u>double bond</u>.
Then, this cyclohexene is hydrogenated to form the cyclohexane.