A. Oxidation of 2° alcohol to a ketone Reagents: Jones Reagent (CrO3 in aquous H₂SO4; acetone)

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II.
Synthesis of Ketones
*
A. Oxidation of 2° alcohol to a ketone
Reagents: Jones Reagent (CrO3 in aquous H₂SO4; acetone)
Reagents: Pyridinium chlorochromate (PCC)
Reagents: Dess-Martin Periodinane; CH₂Cl₂
Reagents: K₂Cr₂O7 in aquous H₂SO4
Reagnets: KMnO4, heat
Reagents: Ozonolysis of Alkenes to aldehydes/ketones
Reagents: Oxymercuration of terminal and internal alkynes; HgSO4,
↓
B.
C.
C.
+ D.
E.
* F.
+
✰ G.
H₂SO4, H₂O
2
H. Reagents: Friedel-Crafts Acylation (Electrohilic Aromatic Substitution);
RC(O)CI, AICI 3
Transcribed Image Text:II. Synthesis of Ketones * A. Oxidation of 2° alcohol to a ketone Reagents: Jones Reagent (CrO3 in aquous H₂SO4; acetone) Reagents: Pyridinium chlorochromate (PCC) Reagents: Dess-Martin Periodinane; CH₂Cl₂ Reagents: K₂Cr₂O7 in aquous H₂SO4 Reagnets: KMnO4, heat Reagents: Ozonolysis of Alkenes to aldehydes/ketones Reagents: Oxymercuration of terminal and internal alkynes; HgSO4, ↓ B. C. C. + D. E. * F. + ✰ G. H₂SO4, H₂O 2 H. Reagents: Friedel-Crafts Acylation (Electrohilic Aromatic Substitution); RC(O)CI, AICI 3
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