Hybridization of carbon in carbonyl group

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SUMMARY

The discussion centers on the hybridization of carbon in the carbonyl group during the reaction of CH3CN with aqueous H2SO4 and water, resulting in acetic acid (CH3COOH) and ammonia (NH3). The participant correctly identifies that the carbon in the carbon-nitrogen triple bond is sp hybridized, while the carbon in the carbon-oxygen double bond is sp2 hybridized. This understanding is crucial for analyzing the molecular structure and reactivity of the compounds involved.

PREREQUISITES
  • Understanding of hybridization concepts in organic chemistry
  • Knowledge of functional groups, specifically carbonyl and amine groups
  • Familiarity with reaction mechanisms involving acids and water
  • Basic grasp of molecular geometry and bonding theories
NEXT STEPS
  • Study the mechanisms of acid-catalyzed reactions in organic chemistry
  • Learn about the properties and reactivity of carbonyl compounds
  • Explore the concept of hybridization in greater detail, focusing on sp and sp2 hybridization
  • Investigate the role of water in organic reactions, particularly in hydrolysis
USEFUL FOR

Chemistry students, organic chemists, and anyone studying reaction mechanisms and hybridization in organic compounds.

xiphoid
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Homework Statement


CH3CN [ in presence of aq. H2SO4 and 2H2O] → CH3COOH + NH3


The Attempt at a Solution


There is a triple bond present between Carbon and nitrogen, hence the first will be sp hybridized, while there is double bond between carbon and oxygen in the second, hence it should be sp2 hydrized, correct?
 
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