The reaction is a typical example of the Williamson ether synthesis method, which involves the formation of an ether from an alkyl halide and an alkoxide ion. This reaction is a nucleophilic substitution where the alkoxide ion attacks the alkyl halide, displacing the halide ion and forming an ether.
The general reaction can be written as:
\(R - X + R - ONa → R - O - R + NaX\)
The Williamson ether synthesis is an important method for preparing ethers in organic chemistry through a nucleophilic substitution mechanism.
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:
A bob of heavy mass \(m\) is suspended by a light string of length \(l\). The bob is given a horizontal velocity \(v_0\) as shown in figure. If the string gets slack at some point P making an angle \( \theta \) from the horizontal, the ratio of the speed \(v\) of the bob at point P to its initial speed \(v_0\) is :
Alcohol is a derivative of water (H2O) that has one, two, or more hydroxyl groups that are attached to a carbon atom of a hydrocarbon chain (an alkyl group). It is one of the most common organic compounds used in sweeteners, fragrances, and medicine.
Read More: Types of Alcohol