Why haloarenes cannot prepare by alcohol?
CBSE, JEE, NEET, CUET
Question Bank, Mock Tests, Exam Papers
NCERT Solutions, Sample Papers, Notes, Videos
Posted by Anisha Kabsuri 4 years, 1 month ago
- 1 answers
Related Questions
Posted by Shivam Modanwal 4 months, 2 weeks ago
- 0 answers
Posted by Mahi Sharma 5 months ago
- 0 answers
Posted by Roshni Gupta 4 months, 4 weeks ago
- 0 answers
Posted by Cinvi Patel 4 months, 3 weeks ago
- 0 answers
Posted by Karan Kumar Mohanta 4 months ago
- 1 answers
Posted by Neha 107 4 months, 2 weeks ago
- 0 answers
Posted by Kashish Baisla 4 months, 4 weeks ago
- 1 answers
Posted by Priya Dharshini B 4 months, 1 week ago
- 4 answers
myCBSEguide
Trusted by 1 Crore+ Students
Test Generator
Create papers online. It's FREE.
CUET Mock Tests
75,000+ questions to practice only on myCBSEguide app
Yogita Ingle 4 years, 1 month ago
Due to resonance in phenol, C— O bond of phenol has some partial double bond character, which strengthens the bond. So, it is difficult to break this C— O bond of phenol while the C— O bond of alcohol is purely single bond and comparatively weaker bond. So, alkyl halides can be prepared by the reaction of alcohols with HCl in the presence of ZnC{{l}_{2}} while aryl halides cannot be prepared by the reaction of phenol with HCl in the presence of ZnCl2.
0Thank You