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10 Cards in this Set
- Front
- Back
What does this do to an alcohol?
Na ----------> Peroxides |
No Conversion of bonds.
Displaces H, leaving O⁻Na⁺ |
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What does this do to an alcohol?
H₃PO₄ ---------> heat |
No Conversion of bonds.
Removes OH Converts single bond on α-β Carbon to double |
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What does this do to a di-alcohol across a single bond?
H₂SO₄ |
No Conversion of bonds.
Loss of one OH Conversion of other OH to double-bond O Pinacol Rearrangement |
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What does this do to a primary alcohol?
H₂CrO₄/H₂O -----------------> acetone |
No Conversion of bonds.
Converts COH to COOH (alcohol to acid) |
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What does this do to a secondary alcohol?
H₂CrO₄/H₂O -----------------> acetone |
No Conversion of bonds.
Converts OH to double-bonded O (alcohol to ketone) |
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What does this do to a primary alcohol?
PCC |
No Conversion of bonds.
Converts alcohol to aldehyde |
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What does this do to a ringed vicinal-diol?
HIO₄ |
Cleaves bond between diols.
OH groups become Carbonyls and H (CHO) |
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What does this do to a Thiol?
O₂ |
No Conversion of bonds.
Converts Thiol to disulfide 2 RSH become RSSR |
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Function on an alcohol
TsCl |
Reverses position of OH (Trans <-> Cis)
ROH + Tscl → ROTs + Nu: → RNu |
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Function for tBuO-
|
Converts alkane to alkene
Removes Br via E2 |