CH 10 Review

Reactions of Alcohols and Thiols from Ch.
10
Jacquie Richardson, Fall 2012 - Page 1
This chapter focuses on things you can do with alcohols and thiols. The main difference
between this and alkyl halide chemistry is that OH is a bad leaving group because its a
strong base. The first few reactions involve converting the -OH into a good leaving group,
which allows them to do most of the reactions out of Ch. 9.
Converting OH to a leaving group

1. The simplest way is to protonate it to OH2, which is a great leaving group because
its neutral once it drops off. To do this, you use strong acid like HX or H2SO4. If
you use H2SO4, theres not really a good nucleophile around so the most likely
outcome is elimination.
This goes by E2 (for primary alcohols) or E1 (for secondary and tertiary).

Remember to check for carbocation rearrangement if its E1. (Note that this is
exactly the same reaction as hydration of an alkene but in reverse.)
You can also use HX (like HCl, HBr, or HI) and protonate the OH, but then there
will be a nucleophile present (X-) so a substitution is more likely. Since this is
under protic conditions, the larger halogens are better at this reaction.
This goes by SN2 (for primary alcohols) or SN1 (for secondary and tertiary).
Again, remember to check for carbocation rearrangement if its E1.
2. The most widely applicable method, and usually the best choice during a
synthesis, is to convert the alcohol to a sulfonate ester.
This creates a group that acts so much like a halogen that sulfonate esters are
often referred to as pseudohalides. This is because their leaving group ability is
about the same as a halogen the pKa of the OS(O2)R group is in the same
range. Mesyl and tosyl are about as good as bromide, and triflyl is slightly better -
about as good as iodide.
Reactions of Alcohols and Thiols from Ch. 10
To install mesyl and tosyl groups, you use the acid chloride plus pyridine.
Pyridine is used to soak up the HCl that gets generated as a byproduct, and
because it catalyzes the reaction.
To install the triflate group, you use triflic anhydride (Tf-O-Tf or Tf2O) plus
pyridine again.
Although we dont look at the mechanism for any of these, its important to note
that the stereochemistry on R will not change during the reaction. The reaction is
being done at O, not C.
Once you have any of these three groups in place of the OH group, you can make
the molecule do any of the alkyl halide chemistry from Ch. 9, exactly as if it were
a real alkyl halide.
E1
R OMs E2
R OTs SN1
R OTf SN2
3. The third way is to use a special halogenating agent. The two options here are
SOCl2 (to convert OH to Cl) and PBr3 (to convert OH to Br). With SOCl2, you
again need pyridine to react with the HCl byproduct.
The mechanism for both of these is roughly the same: the OH group attacks the
other molecule, causing it to drop a halogen. This halogen then comes in and does
SN2 on whatever group the OH has become. We dont look at the full mechanism
of how the OH attaches to the sulfur yet, because it involves S=O chemistry.
For PBr3, though, we do see the whole mechanism.

Since both of these reactions go by SN2, the end result is inversion of

stereochemistry. Also they work well on primary alcohols and okay on secondary,
but not at all on tertiary.
Oxidation and Reduction

This involves changing the amount of partial positive or partial negative charge on an
atom. To find the formal oxidation level of an atom:
1. For every bond an atom has to a less electronegative atom or negative charge, add -1.
2. For every bond an atom has to an equally electronegative atom or radical, add 0.
3. For every bond an atom has to a more electronegative atom or positive charge, add +1.
4. Sum up these numbers for a given atom to find its oxidation level.
We can track changes on a particular atom or atoms during a reaction, to see whether the
molecule as a whole is getting oxidized or reduced. An increase in oxidation level (in
other words, a loss of electron density) is an oxidation; a decrease in oxidation level (in
other words, a gain of electron density) is a reduction.
We can revisit some of the reactions weve seen previously to sort them into categories of
oxidation, reduction, or neither. In this case, you need to sum up the changes across all
affected carbons:
Out of all the alkene additions weve seen, the ones that add 2 non-H groups were all
oxidations, the ones that add 2 Hs were reductions, and the ones that add 1 H and 1 non-
H were neither.
Typical oxidizing agents contain high-electronegativity atoms, often bonded to each other
or to a central, octet-breaking atom. Some examples are Br2, H2O2, CrO3, and O3. Typical
reducing agents contain low-electronegativity atoms, often bonded to each other or to a
central, low-electronegativity atom. Some examples are H2, BH3, and NaBH4.
As a side note, the net oxidation or reduction must be conserved across all species during
a reaction. If an alkene gets oxidized, it is because the other reagents were reduced during
the reaction or vice versa. Many transition metals can exist in various different oxidation
states, so to specify which it is, we use roman numerals in parentheses after the atom.
If a reaction uses Cr (VI) and produces Cr (III), we know that the chromium got reduced
and so the organic molecule must have been oxidized.
Oxidation of Alcohols
This involves changing the oxidation level of the carbon that has the OH on it, by adding
more bonds to O. To do this, the C has to lose bonds to H to make room. (In a few cases,
it can also lose bonds to C, but aside from one case ozonolysis we wont see any
reactions like this for a while.) The ability of the C to get oxidized is therefore dependent
on how many Hs it has to lose, which depends on what type of alcohol it is - 1, 2, or 3.
There are two options available for oxidizing agents.

1. Strong oxidizers: for this, you can use most versions of chromium (VI) attached to
oxygens, in the presence of strong acid. Chromate (H2CrO4 or Na2CrO4/H2SO4),
dichromate (H2Cr2O7 or Na2Cr2O7/H2SO4), or chromium trioxide (CrO3/H2SO4)
will work. Potassium permanganate (KMnO4) will also work but its harsher and
sometimes produces unwanted side reactions. These strong oxidizers will all
oxidize up the molecule as far as possible: 1 alcohols will be become carboxylic
acids and 2 alcohols will become ketones.
Its hard to stop at the aldehyde state, because if theres water present (which
there always is, with these acidic molecules), a side reaction will happen: the
molecule will interconvert rapidly between an aldehyde and a hydrate. This
hydrate acts just like a regular alcohol and gets oxidized further, to the carboxylic
acid state.
2. Weaker oxidizers: if you want to stop at the aldehyde state, you need to use
special chromium (VI) that work in the absence of water. The most common one
is pyridinium chlorochromate (PCC), but pyridinium dichromate (PDC) works
fine too.
Oxidation of Thiols
This is different from oxidation of alcohols, because instead of oxidizing C by
taking away Hs, were actually oxidizing S by making it break the octet rule.
There are several different oxidation states available to sulfur, but we only look at
three of them thiols, disulfides, and sulfonic acids.
To oxidize a thiol to a disulfide, we can use a very mild oxidizer like Br2 or I2.
This also happens very slowly in ambient air, due to oxygen itself being an
oxidizer.
To oxidize a thiol or a disulfide to a sulfonic acid, we need a much stronger

oxidizer like HNO3 or KMnO4.

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Reactions of Alcohols and Thiols from Ch.

Converting OH to a leaving group

This goes by E2 (for primary alcohols) or E1 (for secondary and tertiary).

For PBr3, though, we do see the whole mechanism.

Since both of these reactions go by SN2, the end result is inversion of

Oxidation and Reduction

There are two options available for oxidizing agents.

To oxidize a thiol or a disulfide to a sulfonic acid, we need a much stronger

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