Home
Class 12
CHEMISTRY
The correct order of increasing acidic s...

The correct order of increasing acidic strength is _____.

A

phenol < ethanol < chloroacetic acid < acetic acid

B

ethanol < phenol < chloroacetic acid < acetic acid

C

ethanol < phenol < acetic acid < chloroacetic acid

D

chloroacetic acid < acetic acid < phenol < ethanol

Text Solution

AI Generated Solution

The correct Answer is:
To determine the correct order of increasing acidic strength among the given compounds (phenol, ethanol, chloroacetic acid, and acetic acid), we will analyze the acidic nature of each compound step by step. ### Step 1: Identify the Compounds The compounds given are: 1. Phenol (C6H5OH) 2. Ethanol (C2H5OH) 3. Chloroacetic acid (ClCH2COOH) 4. Acetic acid (CH3COOH) ### Step 2: Understand Acidic Strength Acidic strength is determined by the ability of a compound to donate a proton (H+). The more stable the conjugate base formed after deprotonation, the stronger the acid. ### Step 3: Compare Alcohols and Acids - **Phenol and Ethanol**: Both are alcohols. However, phenol is more acidic than ethanol because the phenoxide ion (the conjugate base of phenol) is stabilized by resonance. In contrast, the ethoxide ion (the conjugate base of ethanol) does not have such stabilization. Thus, we can conclude: \[ \text{Phenol} > \text{Ethanol} \] ### Step 4: Compare Chloroacetic Acid and Acetic Acid - **Chloroacetic Acid vs. Acetic Acid**: Chloroacetic acid has a chlorine atom, which is an electron-withdrawing group. This group stabilizes the conjugate base (the chloroacetate ion) through its -I effect, making it easier to lose the proton. Acetic acid, on the other hand, does not have such an electron-withdrawing group and is therefore less acidic. Thus, we can conclude: \[ \text{Chloroacetic Acid} > \text{Acetic Acid} \] ### Step 5: Final Comparison Now we can summarize the acidic strength of the compounds: 1. Ethanol (least acidic) 2. Phenol 3. Acetic Acid 4. Chloroacetic Acid (most acidic) ### Step 6: Order of Increasing Acidity Putting it all together, the correct order of increasing acidic strength is: \[ \text{Ethanol} < \text{Phenol} < \text{Acetic Acid} < \text{Chloroacetic Acid} \] ### Final Answer The correct order of increasing acidic strength is: **Ethanol < Phenol < Acetic Acid < Chloroacetic Acid** ---
Promotional Banner

Topper's Solved these Questions

  • ALDEHYDES, KETONES AND CARBOXYLIC ACIDS

    NCERT FINGERTIPS ENGLISH|Exercise ASSERTION & REASON|15 Videos
  • ALDEHYDES, KETONES AND CARBOXYLIC ACIDS

    NCERT FINGERTIPS ENGLISH|Exercise Nomenclature And Structure Of Carbonyl Group|3 Videos
  • ALDEHYDES, KETONES AND CARBOXYLIC ACIDS

    NCERT FINGERTIPS ENGLISH|Exercise MCQs(CHEMICAL REACTIONS )|18 Videos
  • ALCOHOLS,PHENOLS AND ETHERS

    NCERT FINGERTIPS ENGLISH|Exercise Assertion And Reason|14 Videos
  • AMINES

    NCERT FINGERTIPS ENGLISH|Exercise ASSERTION & REASON CORNER|14 Videos

Similar Questions

Explore conceptually related problems

Select the correct alternative from the choices given : The correct order of increasing acidic strength of the oxoacids of chlorine is :

Arrange in order of increasing acidic strength

Give the correct order of the increasing acidic strength of the following compounds :

The correct order of increasing acid strength of the compounds is (a). CH_(3)CO_(2)H (b). MeOCH_(2)CO_(2)H (c) CF_(3)CO_(2)H (d)

Arrange in the order of increasing acidic strengths.

The correct order of decreasing acidic strength of oxyacids of group 15 elements is

The correct decreasing order for acid strength is :