Home
Class 11
CHEMISTRY
Why pyridine is a much weaker base than ...

Why pyridine is a much weaker base than aliphatic amines ?

Text Solution

Verified by Experts

Pyridine is a weaker base than `R (##KSV_ORG_P1_C04_E01_007_S02##) NH_(2)` due to +I effect in aliphatic amine (aliphatic amine gt aromatic amine).
Promotional Banner

Topper's Solved these Questions

  • GENERAL ORGANIC CHEMISTRY

    CENGAGE CHEMISTRY|Exercise Concept|16 Videos
  • GENERAL ORGANIC CHEMISTRY

    CENGAGE CHEMISTRY|Exercise Comprehension|20 Videos
  • GENERAL ORGANIC CHEMISTRY

    CENGAGE CHEMISTRY|Exercise Solved Example|18 Videos
  • CLASSIFICATION AND NOMENCLATURE OF ORGANIC COMPOUNDS

    CENGAGE CHEMISTRY|Exercise Analytical and Descriptive Type|3 Videos
  • HYDROGEN, WATER AND HYDROGEN PEROXIDE

    CENGAGE CHEMISTRY|Exercise Subjective Archive (Subjective)|3 Videos

Similar Questions

Explore conceptually related problems

(i) What is Gabriel phthalimide synthesis? Why aromatic primary amines cannot be prepared by this method? (ii) Why are aromatic amines weaker bases than aliphatic amines?

Why o-derivative is weaker base than aniline?

Why is carbon nitrogen bond length in aromatic amines shorter than in aliphatic amines?

Why is carbon-nitrogen bond length in aromatic amines shorter than in aliphatic amines?

Give reason: Aniline is a weaker base than cyclohexylamine.

p-methoxyaniline is a stronger base than aniline but p-nitroaniline is a weaker base than aniline. Explain.

Assertion : p-nitroaniline is a weaker base than p-toluidine. Reason: The electron donating -NO_(2) group in p-nitroaniline makes it a weaker base.