Organic Conversions with Answers

Organic conversions refer to chemical reactions or processes in which one organic compound is transformed into another through the manipulation of its chemical structure. There are numerous types of organic conversions, each serving specific purposes in organic synthesis, drug discovery, materials science, and other fields. Here are some common types of organic conversions along with examples:

  1. Functional Group Interconversions: These conversions involve changing one functional group into another. For instance:
    • Conversion of alcohols to alkyl halides through substitution reactions.
    • Oxidation of alcohols to aldehydes or ketones.
    • Reduction of carbonyl compounds to alcohols.
    • Halogenation of alkenes to form alkyl halides.
  2. Protection and Deprotection Reactions: In multi-step synthesis, protecting groups are often used to temporarily block certain functional groups, preventing them from reacting during subsequent steps. Examples include:
    • Acetal formation to protect carbonyl groups.
    • Silyl ether formation to protect alcohols.
    • Deprotection of acetals or silyl ethers using acidic conditions.
  3. Carbon-Carbon Bond Formation: These conversions involve the formation of new carbon-carbon bonds. Examples include:
    • Aldol condensation to form β-hydroxy carbonyl compounds.
    • Grignard reaction to form carbon-carbon bonds between an organomagnesium halide and a carbonyl compound.
    • Heck reaction for the formation of carbon-carbon bonds between aryl or vinyl halides and alkenes.
  4. Rearrangement Reactions: These involve the rearrangement of atoms within a molecule to form a different structural isomer. Examples include:
    • Wagner-Meerwein rearrangement involving migration of a hydride, alkyl, or aryl group.
    • Beckmann rearrangement converting oximes to amides.
    • Claisen rearrangement leading to the rearrangement of allyl vinyl ethers to form allyl ketones.
  5. Ring-Opening and Ring-Closing Reactions: These conversions involve breaking or forming cyclic structures. Examples include:
    • Ring-opening of epoxides with nucleophiles to form diols.
    • Ring-closing metathesis (RCM) for the synthesis of cyclic compounds using olefin metathesis.
    • Diels-Alder reaction for the formation of cyclic compounds from dienes and dienophiles.

These are just a few examples of the many organic conversions used in organic chemistry. Each type of conversion offers a unique way to modify or synthesize organic molecules for various applications.

We have tried to provide some common organic conversions –

  1. Acetic acid to propanoic acid
  2. Acetaldehyde to propanal
  3. Ethyl bromide to n-propyl bromide
  4. methyl iodide to ethyl iodide
  5. .
  6. .
  7. Methanol to acetone
  8. Ethanol to propanone
  9. Propanone to propene
  10. Ethanol to ethane diol
  11. ethanol to 1,1-dichloro ethane
  12. Alkyl halide to ether
  13. Methyl bromide to ethyl amine
  14. 1-propanol to 2-propanol
  15. 2-propanol to 1-propanol
  16. Isopropyl alcohol to tert alcohol
  17. .
  18. ethanol to 1-propanol
  19. Propanoic acid to acetic acid
  20. Formic acid to acetic acid
  21. Propanal to ethane
  22. Propene to 1-propyl alcohol
  23. Acetic acid to butane
  24. Acetaldehyde to methyl bromide
  25. Acetaldehyde to crotonaldehyde
  26. Acetaldehyde to acetone
  27. Acetaldehyde to formaldehyde
  28. Acetaldehyde to ethyl amine
  29. Ethyne to acetic acid
  30. Methane to ethanol
  31. Acetic acid to acetaldehyde
  32. Methane to acetone
  33. Acetic acid to ethyl amine
  34. Acetic acid to methyl alcohol
  35. .
  36. Isocyanide to secondary amine
  37. Acetaldehyde to butane-1,3-diol
  38. Ethanol to 3-hydroxy butanal
  39. Methyl bromide to acetic acid
  40. Nitrobenzene to benzoic acid
  41. Aniline to benzylalcohol
  42. Nitrobenzene to iodobenzene
  43. Aniline to chlorobenzene
  44. Aniline fluorobenzene
  45. Aniline to benzene
  46. Aniline to phenyl cyanide
  47. Aniline to benzoic acid
  48. Nitrobenzene to benzene
  49. Nitrobenzene to 2,4,6-tribromo aniline
  50. Benzaldehyde to acetophenone
  51. Ethyl alcohol to diethyl ether
  52. Propanoic acid to 3-pentanone
  53. Benzaldehyde to benzophenone
  54. Benzaldehyde to cyanobenzene
  55. Benzaldehyde to cinnammic acid
  56. Benzaldehyde to nitrobenzene
  57. Benzoic acid to aniline
  58. Benzoic acid to benzaldehyde
  59. Benzoic acid to phenyl cyanide
  60. Benzoic acid to benzamide
  61. Salicylic acid to benzene
  62. Benzene to diphenyl
  63. Benzoic acid to benzyl chloride
  64. Benzene to diazonium chloride
  65. Benzene to m-nitroacetophenone
  66. Benzene to benzaldehyde
  67. Nitrobenzene to anisole
  68. Phenol to picric acid
  69. Benzene to DDT
  70. Phenol to aspirin
  71. Phenol to methyl salicylate
  72. Aniline to acetanilide
  73. Benzaldehyde to 3-phenylpropan-1-ol
  74. Benzaldehyde to Mandelic acid
  75. Bromobenzene to 1-phenylethanol
  76. Benzoic acid to m-nitrobenzyl alcohol
  77. Bromobenzene to benzoic acid
  78. Benzene to methyl benzoate
  79. Aniline to p-bromoaniline
  80. Benzamide to toluene
  81. Benzoic acid to phenol
  82. Phenol to acetophenone
  83. Benzene to benzophenone
  84. Phenol to benzoic acid
  85. Aniline to p-hydroxyazobenzene
  86. Nitrobenzene to p-aminobenze
  87. Bromobenzene to m-nitrobenzoic acid
  88. Benzene to benzoic acid
  89. Benzene to aniline
  90. Benzene to anisole
  91. Benzene to m-chloro aniline
  92. Benzene to benzyl alcohol
  93. Benzene to m-nitro aniline
  94. Toluene to 3-nitro benzoic acid
  95. Benzene to phenol
  96. Ethanol to Propanone
  97. Ethyl alcohol to ethylene glycol
  98. Propan-2-ol to ethylene glycol
  99. Propan-2-ol to 1-bromopropane
  100. Ethyl alcohol to tertiary butyl alcohol
  101. n-Propyl alcohol to isopropyl alcohol
  102. isopropyl alcohol to n-propyl alcohol
  103. Acetylene to n-butyl alcohol
  104. Ethylene oxide to n-propyl alcohol
  105. n-butyl alcohol to dimethyl acetylene
  106. n-propyl alcohol to n-hexane
  107. Methyl alcohol to isopropyl alcohol
  108. Ethyl bromide to methane
  109. Ethyl alcohol to n-butyric acid
  110. Ethyl alcohol to vinyl acetate
  111. Acetone to tertiary butyl alcohol
  112. Ethyl alcohol to isopropyl alcohol
  113. Methyl iodide to methyl ethyl ether
  114. Ethylene to divinyl ether
  115. Dimethyl ether to diethyl ether
  116. Propene to 2-ethoxypropane
  117. Ethyl iodide to diethylether
  118. Ethanal to lactic acid
  119. Acetaldehyde to acetone
  120. Ethanal to ethyne
  121. Ethanal to 2-hydroxy but-3-enoic acid
  122. Formaldehyde to n-butane
  123. Ethanol to Butan-2-one
  124. Acetaldehyde to Crotonic acid
  125. Propanal to Propyne
  126. Acetone to Phorone
  127. 1-bromopropane to butanoic acid
  128. Ethyne to propanoic acid
  129. Ethanol to phenyl ethanal
  130. Propanone to iodoform
  131. Formaldehyde to urotropine
  132. Acetone to tertiary butyl alcohol
  133. Ethanal to propan-2-ol
  134. Acetylene to Acetic acid
  135. Acetic acid to Glycine
  136. Formic acid to oxalic acid
  137. Propionic acid to n-butylamine
WhatsApp Image 2024 03 24 at 9.36.47 PM 10 ALL ABOUT CHEMISTRY
WhatsApp Image 2024 03 24 at 9.36.47 PM 9 ALL ABOUT CHEMISTRY
WhatsApp Image 2024 03 24 at 9.36.47 PM 8 ALL ABOUT CHEMISTRY
WhatsApp Image 2024 03 24 at 9.36.47 PM 7 ALL ABOUT CHEMISTRY
WhatsApp Image 2024 03 24 at 9.36.47 PM 6 1 ALL ABOUT CHEMISTRY
WhatsApp Image 2024 03 24 at 9.36.47 PM 5 ALL ABOUT CHEMISTRY
WhatsApp Image 2024 03 24 at 9.36.47 PM 4 ALL ABOUT CHEMISTRY
WhatsApp Image 2024 03 24 at 9.36.47 PM 3 ALL ABOUT CHEMISTRY
WhatsApp Image 2024 03 24 at 9.36.47 PM 2 ALL ABOUT CHEMISTRY
WhatsApp Image 2024 03 24 at 9.36.47 PM 1 ALL ABOUT CHEMISTRY
WhatsApp Image 2024 03 24 at 9.36.47 PM ALL ABOUT CHEMISTRY
WhatsApp Image 2024 03 24 at 9.36.46 PM 1 ALL ABOUT CHEMISTRY
WhatsApp Image 2024 03 24 at 9.36.46 PM ALL ABOUT CHEMISTRY

error: Content is protected !!