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Textbook Notes for Paul Harrison

MCMASTERCHEM 2OB3Paul HarrisonSummer

CHEM 2OB3 Chapter Notes - Chapter 12: Pi Bond, Ozonolysis, Leaving Group

Ashley Eugine2 Page
26 Jul 2015
21
Refer to chapter 9 and chapter 10 reagents for one- step alkene and alkyne reactions. Reagents must be considered to ensure a anti/mark product is achi
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MCMASTERCHEM 2OB3Paul HarrisonSummer

CHEM 2OB3 Chapter Notes - Chapter 17: Allyl Group, Tautomer, Sigma Bond

Ashley Eugine5 Page
26 Jul 2015
64
Double bonds are connected to the same c. Sterically hindered bases (t-buok) allows only emilination reactions to occur. Conjugated systems have lower
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MCMASTERCHEM 2OB3Paul HarrisonSummer

CHEM 2OB3 Chapter Notes - Chapter 13: Sodium Borohydride, Hydroxy Group, Phosphorus Tribromide

Ashley Eugine8 Page
26 Jul 2015
29
Cyclic alcohols: phenol" can be used as the. Miscibility: (except methanol) regions via h-bonding o chain) = solubility. Except butanol is consider sol
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MCMASTERCHEM 2OB3Paul HarrisonSummer

CHEM 2OB3 Chapter Notes - Chapter 14: Partial Charge, Alkoxy Group, Sodium Borohydride

Ashley Eugine8 Page
26 Jul 2015
29
Side groups to the left and right of the ether. Chains to the left and right of the ether. Name the parent chain and the alkoxy substituent (includes t
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MCMASTERCHEM 2OB3Paul HarrisonSummer

CHEM 2OB3 Chapter Notes - Chapter 11: Pi Bond, Chloroform, Thermodynamics

Ashley Eugine7 Page
26 Jul 2015
39
Draw all possible radicals with c h homolytic cleavage. Label: 1", 2", 3", allylic and vinylic. Sp2 trigonal planar due to empty p-orbital (carbocation
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