Home
Class 12
CHEMISTRY
On reacting chloral hydrate with NaOH th...

On reacting chloral hydrate with NaOH the products obtained is/are:

A

`CHCl_(3)`

B

HCOONa + `H_(2)`O

C

Both (1) and (2)

D

none of these

Text Solution

AI Generated Solution

The correct Answer is:
To solve the question regarding the reaction of chloral hydrate with NaOH, we will follow these steps: ### Step 1: Identify the Structure of Chloral Hydrate Chloral hydrate is derived from chloral (CCl₃CHO) and water. The structure of chloral hydrate can be represented as: \[ \text{CCl}_3\text{CHOH}_2 \] This compound is a geminal diol, where the carbonyl group (C=O) of chloral is converted into a hydroxyl group (–OH) upon reaction with water. **Hint:** Remember that chloral hydrate is formed from chloral and water, leading to a stable geminal diol structure. ### Step 2: Understand the Role of NaOH Sodium hydroxide (NaOH) is a strong base that dissociates in solution to provide hydroxide ions (OH⁻). These hydroxide ions will act as nucleophiles in the reaction. **Hint:** Recognize that NaOH provides OH⁻ ions which can attack electrophilic centers in organic molecules. ### Step 3: Nucleophilic Attack The hydroxide ion (OH⁻) will attack the carbon atom of the carbonyl group in chloral hydrate. This carbon is electrophilic due to the presence of the electronegative chlorine atoms. **Hint:** Focus on the mechanism of nucleophilic attack where OH⁻ targets the electrophilic carbon. ### Step 4: Formation of a Tetrahedral Intermediate The attack of the hydroxide ion leads to the formation of a tetrahedral intermediate. This intermediate will have a negative charge on the carbon that was previously part of the carbonyl group. **Hint:** Tetrahedral intermediates are common in nucleophilic addition reactions. ### Step 5: Departure of the Leaving Group In this case, the CCl₃ group (trichloromethyl group) acts as a good leaving group due to the stabilizing effect of the three chlorine atoms. When the CCl₃ group leaves, it forms a trichloromethyl anion (CCl₃⁻). **Hint:** Remember that good leaving groups are often stabilized by resonance or inductive effects. ### Step 6: Formation of Products After the CCl₃ group leaves, the remaining structure will rearrange, leading to the formation of chloroform (CHCl₃) and sodium formate (HCOO⁻Na). The reaction also produces water as a byproduct. **Hint:** Identify the final products by considering the stability and reactivity of the remaining groups after the leaving group departs. ### Final Answer The products obtained from the reaction of chloral hydrate with NaOH are: - Chloroform (CHCl₃) - Sodium formate (HCOO⁻Na) - Water (H₂O) ### Summary of Products 1. **Chloroform (CHCl₃)** 2. **Sodium Formate (HCOO⁻Na)** 3. **Water (H₂O)**
Promotional Banner

Similar Questions

Explore conceptually related problems

Bromine react with NaOH to produce

When Zn is treated with excess of NaOH, the product obtained is

When ferric oxide reacts with NaOH , the product formed is

If phospheric acid is allowed to react with sufficient quantity of NaOH , the product obtained is

When nitrobenzene is reduced with zinc and methanolic NaOH the product obtained is .

If 1,3- dibromopropane reacts with zinc and NaI, the product obtained is :

When phenol reacts with benzene diazonium chloride , the product obtained is :

P_(4)+NaOH undeset("warm") to Products. Explaine the reducing character of one of the products obtained by taking the example of copper sulphate.