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1° and 2° alcohols (OH) can be made by... - Reduc on
3° alcohols... - Cannot be made if reducing agent is a hydride [H⁻] source
LiAlH₄ - Strong reducing agent
NaBH₄ - Weak reducing agent
PCC - Weak oxidizing agent
PCC oxidizes 1° and 2° alcohols respec vely into an... - Aldehyde and/or ketone
KMnO₄ - Strong oxidizing agent
H₂Cr₂O₇ - Strong oxidizing agent
All 2° OH stop at ketone when using... - H₂Cr₂O₇ and heat
R-C-OH → R-C=O-H → R-C=O-OH - Stepwise Oxida on
Carbon atom oxidized must have at least one... - hydrogen atom
, >=< → >=O + O=< - 1. O₃ (Ozone) and 2. Me₂S (Dimethyl Sulfide)
IR: R-OH - Broad and centered ~3400cm⁻¹
Organometallics... Carbon is a _____ - Nucleophile
Organometallics are strong _____ - Bases
MgBr, MgCl, MgI are _____ - Grignard reagents
Retrosynthesis - Breaking down target molecule into simple star ng materials
TMSCL and TBSCL... - Are protec ng groups
Radical Subs tu on - Mechanism contains 3 major steps: 1. Ini a on, 2. Propaga on, 3.
Termina on
Allyl (=-·) - Most stable, followed by... Benzyl > 3° C⁺ > 2° C⁺ > 1° C⁺ >>> Vinyl (=·)
Vinyl (=·) - Least stable
1, 2 - addi on product... - Kine c
1, 4 - addi on product... - Thermodynamic
1, 4 - subs tuted - Para - posi on