Answer:
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The concentration of [H3O⁺]=2.86 x 10⁻⁶ M
<h3>Further explanation</h3>
In general, the weak acid ionization reaction
HA (aq) ---> H⁺ (aq) + A⁻ (aq)
Ka's value
![\large {\boxed {\bold {Ka \: = \: \frac {[H ^ +] [A ^ -]} {[HA]}}}}](https://tex.z-dn.net/?f=%5Clarge%20%7B%5Cboxed%20%7B%5Cbold%20%7BKa%20%5C%3A%20%3D%20%5C%3A%20%5Cfrac%20%7B%5BH%20%5E%20%2B%5D%20%5BA%20%5E%20-%5D%7D%20%7B%5BHA%5D%7D%7D%7D%7D)
Reaction
HC₂H₃O₂ (aq) + H₂O (l) ⇔ (aq) + H₃O⁺ (aq) Ka = 1.8 x 10⁻⁵
![\tt Ka=\dfrac{[C_2H_3O^{2-}[H_3O^+]]}{[HC_2H_3O_2]}}\\\\1.8\times 10^{-5}=\dfrac{0.22\times [H_3O^+]}{0.035}](https://tex.z-dn.net/?f=%5Ctt%20Ka%3D%5Cdfrac%7B%5BC_2H_3O%5E%7B2-%7D%5BH_3O%5E%2B%5D%5D%7D%7B%5BHC_2H_3O_2%5D%7D%7D%5C%5C%5C%5C1.8%5Ctimes%2010%5E%7B-5%7D%3D%5Cdfrac%7B0.22%5Ctimes%20%5BH_3O%5E%2B%5D%7D%7B0.035%7D)
[H₃O⁺]=2.86 x 10⁻⁶ M
Answer:
The pair of arrows which represents the relationship of speeds of the two cars is;
The second option as shown in the attached drawing
Explanation:
The given parameters are;
The reading on the speedometer of one car = 20 m/s
The reading on the speedometer of the other car = 72 km/h = 20 m/s
The blue arrow = 20 m/s
Therefore, given that the speeds of both cars are equal (20 m/s = 72 km/h = 20 m/s), the pair of arrows that represent the relationship of speeds of the two cars is two equal length blue arrows which is the second option
The attached diagram showing the pair of arrows that represents the relationship of speeds of the two cars is drawn using Microsoft Visio.
Answer:
IV
Explanation:
The complete question is shown in the image attached.
Let us call to mind the fact that the SN1 mechanism involves the formation of carbocation in the rate determining step. The order of stability of cabocations is; tertiary > secondary > primary > methyl.
Hence, a tertiary alkyl halide is more likely to undergo nucleophilic substitution reaction by SN1 mechanism since it forms a more stable cabocation in the rate determining step.
Structure IV is a tertiary alkyl halide, hence it is more likely to undergo nucleophilic substitution reaction by SN1 mechanism.