Answer:
a. Phosphoric Acid
b. Acetic Acid
c. Hypochlorous Acid
Explanation:
A buffer works when the pH of this one is in pKa ± 1. That means, to find which buffer system works in some pH you need to find pKa:
pKa = -log Ka
<em>pKa Acetic acid:</em>
-log1.8x10⁻⁵ = 4.74
<em>pKa phosphoric acid:</em>
-log7.5x10⁻³ = 2.12
<em>pKa hypochlorous acid:</em>
-log3.5x10⁻⁸ = 7.46
a. For a pH of 2.8 the best choice is phophoric acid because its effective range is: 1.12 - 3.12 and 2.8 is between these values.
b. pH 4.5. Acetic acid. effective between pH's 3.74 - 5.74
c. pH 7.5. Hypochlorous acid that works between 6.46 and 8.46
If you have a book, read it!! I promise you, it tells you this answer!
The angle- angle similarity postulate. It states that if a triangle has two equal corresponding angles the angles are similar.
Chemical properties include reactivity with other elements of substances, toxicity, flammability, and chemical stability
just to name a few
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.
