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27 Cards in this Set
- Front
- Back
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H2SO4 and H2O |
H2SO4 donates H to H2O making it H3O+, good proton donor |
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H2SO4, H2O |
Alkyne or alkene to a ketone or alcohol. Epoxide to add two trans alcohol groups. |
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PCC |
2 Alcohol to ketone, 1 Alcohol to aldehyde |
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mCPBA |
Alkene to epoxide |
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H20, H+ |
Epoxide to trans 2 OH |
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NaOH, H2O |
Epoxide to trans 2 OH |
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O3, H2O |
Oxidative cleavage of Alkyne to carboxylic acids |
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NaNH2 |
Deprotanates alkyne |
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CH3Br |
Donates CH3s to an Alkyne |
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OsO4, NaHSO3, H2O |
Alkene syn hydroxilation (add 2 OH) |
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O3, (CH3)2S |
Alkene oxidative cleavage |
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H2, Lindlar's Catalyst |
Alkyne to alkene to alkane |
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O3, H2O |
Oxidative cleavage of Alkyne |
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NaNH2 |
Deprotanates alkyne |
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CH3Br |
Donates CH3s to an Alkyne |
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OsO4, NaHSO3, H2O |
Alkene to trans 2 OH |
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O3, (CH3)2S |
Alkene oxidative cleavage |
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H2, Lindlar's Catalyst |
Alkyne to alkene to alkane |
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Na, NH3 |
Alkyne to alkene |
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tBuOK, H2, Pd/C |
Haloalkane to alkane |
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LiAlH4, H2O |
Haloalkane to alkane, or epoxide to alcohol |
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H2, Pd/C |
Alkyne to alkene to alkane |
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NaNH2, /\/Br |
Terminal alkyne to internal alkyne
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Na2Cr2O7, H2SO4 |
alcohol to ketone |
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Add more carbons to an alkyne |
react with two equivalents of HBr to make an alkene, then react with H2 and PdC to create a haloalkane |
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H2, PdC |
Reduces alkene to alkane |
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NaNH2, epoxide |
epoxide ring opens and can be added to the deprotonated alkyne |
