Here's the rationale behind this order:
1. Carboxylic acids (RCOOH) are strong acids because they can donate a proton (H+) readily due to the presence of the carboxyl group (COOH). They have a dissociable hydrogen ion (H+), making them stronger acids than the other compounds listed.
2. Water (HOH) is also a strong acid but not as strong as carboxylic acids. Water can act as an acid by donating a proton (H+) to another molecule or ion, but it is weaker than carboxylic acids in this regard.
3. Alcohols (ROH) are weaker acids than both carboxylic acids and water. While they can donate a proton, it's less likely to occur compared to carboxylic acids and water.
4. Alkynes (HC ≡ CH) are the weakest acids among the listed compounds. They are not acidic under normal conditions and do not readily donate protons.
So, the correct order is (B): RCOOH > HOH > ROH > HC ≡ CH.
The order of acidity of the following compounds is:
(i) o-Nitrophenol
(ii) Phenol
(iii) o-Cresol
(iv) Ethanol
Given below are two statements:
Statement I: Dimethyl ether is completely soluble in water. However, diethyl ether is soluble in water to a very small extent.
Statement II: Sodium metal can be used to dry diethyl ether and not ethyl alcohol.
In the light of the given statements, choose the correct answer from the options given below:
AB is a part of an electrical circuit (see figure). The potential difference \(V_A - V_B\), at the instant when current \(i = 2\) A and is increasing at a rate of 1 amp/second is:
Read More: Alcohols, Phenols, and Ethers