Answer:
The formula of Organic acid is as follow,
R-COOH
Explanation:
The class of organic acids is called Carboxylic Acids. In above general structure, R is alkyl group and can vary. While -COOH is the functional group.
Carboxylic Acids has the tendency to loose protons and their pKa value depends upon the alkyl group. For example the pKa value of Acetic acid (R = -CH₃) is 4.7. The driving force for this acidity is the stability of carboxylate (conjugate base) due resonance. i.e
RCOOH ⇄ RCOO⁻ + H⁺
Where;
RCOO⁻ = Carboxylate Ion (Conjugate base)
Answer:
b,d
Explanation:
An ion is an atom with a difference in the amount of protons and elektrons.
Answer:
3.76 x 1014 s-1? λ = c/ν = 3.00 x 108 m/s = 7.98 x 10-7 m 3.76 x 1014 s-1.
Explanation:
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Given the molar mass of Nitrogen is 14.01g/mol you can use that to solve for the moles of nitrogen.
0.235g(1mol/14.01g) = .0168 moles.
Answer:
Fewer hydrogen bonds form between alcohol molecules. As a result, less heat is needed for alcohol molecules to break away from solution and enter the air.
Explanation:
Hydrogen bonding is a kind of intermolecular interaction that occurs when hydrogen is bonded to a highly electronegative atom.
Both water and alcohols exhibit hydrogen bonding. However, alcohols exhibit fewer hydrogen bonds than water.
As a result of this, the temperature of evaporation is much higher for water than for alcohol because hydrogen bonds hold water molecules more closely than alcohol molecules are held.
