Organic Reactions Visual Guide

knoevenagal reaction n.w
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Explore a visual guide showcasing the Knoevenagel reaction, Mannich reaction, Witting's reaction, and their mechanisms step by step. Understand the condensation of methanol, formation of iminium ion, ylides attack, and more in organic chemistry reactions.

  • Organic Chemistry
  • Reaction Mechanisms
  • Chemical Reactions
  • Visual Guide
  • Knoevenagel

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Presentation Transcript


  1. Knoevenagal reaction

  2. Mechanism

  3. Step 1-2 as explained in other reactions

  4. Step 3: protonation: - alkoxide accepts a proton to form hydroxyl compound.

  5. Step 4: involves dehydration

  6. Mannich reaction

  7. Reaction involves condensation of methanol which amine p an active methylene compound to form a Mannich base.

  8. Mechanism:-

  9. Step 1: formation of Imminium ion

  10. Step 2: formation of carbanion

  11. Step 3: attack by carbanion

  12. Wittings reaction

  13. Reaction occurs between an aldehyde/ketone and phosphorous ylides to form substituted alkenes.

  14. Phosphorous ylide is prepared by reacting a base with an alkyl triphenyl phosphonium halide as shown below

  15. Mechanism

  16. Step 1: attack by ylides

  17. Structure B acts as the carbanion and initiates the nucleophilic attack on the carbonyl carbon to form betaine

  18. Step 2: elimination of triphenyl phosphate oxide to yield an alkenes

  19. In elimination reactions, atoms or groups are removed from a reactant.

  20. removed from a carbon and a hydrogen is removed from an adjacent carbon, a double bond is formed below the 2 carbons from which the atoms are removed e.g.

  21. CH3 CHCH2CH3+ CHO3- CH3CH =CH CH2CH3

  22. Generally,

  23. CH3 CH2CH2X + Y-CH3CH2CH2Y + X-

  24. Substitution reaction

  25. CH3CH=CH2+ HY + X-(elimination reaction)

  26. Factors affecting elimination reaction

  27. Structure of the alkyl halide (RX)

  28. reaction proceeds through an intermediate of secondary carbocation which rearranges to the more stable tertiary carbocation. Base removes proton from - carbon.

  29. Primary, secondary and tertiary alkyl halides undergo E2 reactions. It is a one step mechanism involving bond breaking and bond formation.

  30. Text for further reading

  31. Organic chemistry Brief course by Robert Atkins and Francis. A. Carey

  32. Organic reaction mechanism, conversions and problems by R.L Madan

  33. Because the bowling ball is raised to a greater height above the ground, its potential energy increases.

  34. lifted a distance of 1.6 m. To calculate the work performed to raise the ball, we use both Equation 5.3 and for the force that is due to gravity:

  35. (5.4 kg)(9.8m/s2)(1.6m)=85 kg- m2/s2=85j

  36. When the ball is dropped, its potential is converted to kinetic energy. At the instant just before

  37. the ball hits the ground, we assume that the kinetic energy is equal to the work done in part(b), 85j:

  38. Heat= (4.50 g CH4)(= -250j

  39. H = -196 kj

  40. H = -393.5kJ

  41. H = -283.0kJ

  42. H = -393.5kJ (i)

  43. H = -283.0kJ (ii)

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