For this question, I think it is the other way around. It is true that chloroacetic acid is stronger in strength than acetic acid. Acid strength is measured as the equilibrium constant of the reaction <span>HA -----> H+ + A-
</span><span> In acetic acid, the anion produced by dissociation is CH3-COO-; in chloroacetic acid it is CH2Cl-COO-. Comparing the two, in the first one the negative charge is taken up mostly by the two oxygen atoms. In the second there is also an electronegative chlorine atom nearby to draw more charge towards itself. Therefore, the charge is less concentrated in the chloroacetate ion than it is in the acetate ion, and, accordingly, chloroacetic acid is stronger than acetic acid. </span>
Answer:
The volumetric ratio is 0,71
Explanation:
Let's begin with the equation:
(1)
Where:
Db: Blend Density, Mb: Blend Mass and Vb: Blend Volume
And we know:
(2)
Where:
Vg: Gasoline Volume and Vk: Kerosene Volume
Therefore replacing (2) into (1):

(3)
Where:
Dg: Gasoline Density and Dk: Kerosene Density
The specific gravity is defined as:

Therefore:

Where:
Dref: Reference Density
SGb: Blend Specific Gravity
SGg: Gasoline Specific Gravity (which is 0.7 approximately)
SGk: Kerosene Specific Gravity
Replacing these equations into (3) we get:





Replacing with the Specific Gravity data, we obtain:





Answer:
attached below
Explanation:
Structure of two acyclic compounds with 3 or more carbons that exhibits one singlet in 1H-NMR spectrum
a) Acetone CH₃COCH₃
Attached below is the structure
b) But-2-yne (CH₃C)₂
Attached below is the structure