Todd:Chem3x11 ToddL4

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=Chem3x11 Lecture 4=
=Chem3x11 Lecture 4=
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Under construction Sat Apr 28.<br>
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This is a general lecture on mechanisms, molecular orbitals and reactive intermediates.<br>
(Back to [[Todd:Teaching | the main teaching page]])
(Back to [[Todd:Teaching | the main teaching page]])
==Key concepts==
==Key concepts==
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* 1
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* Molecular orbitals impose geometrical restrictions on reaction mechanisms
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* The stereochemical outcome of a reaction can tell is a lot about a reaction mechanism
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* Intermediates like carbocations, carbanions and radicals can destroy the stereochemical integrity of enantiopure starting materials
==Why do we Study Reaction Mechanisms?==
==Why do we Study Reaction Mechanisms?==
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When we consider factors that promote an S<sub>N</sub>1 reaction we are allowed to consider things that stabilise the carbocation. Note that this is an approximation - what we ought to be doing is considering things that stabilise the ''transition state'' leading ''to'' the carbocation. The ''Hammond Postulate'' tells us that because the carbocation is fairly high in energy compared to the species either side, the transition states will resemble the carbocation itself. What factors favour S<sub>N</sub>1 processes? Obvious things like polar solvents, adjacent π systems and adjacent lone pairs. Adjacent carbonyl groups do not - it turns out the only orbital that can interact with the carbocation is the C=O π* orbital, but since these are both empty there is no stabilization.
When we consider factors that promote an S<sub>N</sub>1 reaction we are allowed to consider things that stabilise the carbocation. Note that this is an approximation - what we ought to be doing is considering things that stabilise the ''transition state'' leading ''to'' the carbocation. The ''Hammond Postulate'' tells us that because the carbocation is fairly high in energy compared to the species either side, the transition states will resemble the carbocation itself. What factors favour S<sub>N</sub>1 processes? Obvious things like polar solvents, adjacent π systems and adjacent lone pairs. Adjacent carbonyl groups do not - it turns out the only orbital that can interact with the carbocation is the C=O π* orbital, but since these are both empty there is no stabilization.
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==Carbanions and Stereochemistry==
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Take an enantiopure alkyl halide and make a Grignard out of it and you will be sorely disappointed in the enantiomeric excess of the product of your reaction with that Grignard.
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[[Image:Grignard Scramble.png|thumb|center|400px| '''Scheme 12:''' Formation of a Grignard Gives a Racemate in the Reaction Product]]
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Carbanions don't (usually) retain their stereochemical integrity, which is kind of annoying actually.
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[[Image:Grignard Scramble Mechanism.png|thumb|center|400px| '''Scheme 13:''' Stereochemical Scrambling of a Grignard Reagent]]
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The same thing holds for many carbanions, particularly if the charge is somehow stabilized.
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[[Image:Carbanions Planar.png|thumb|center|400px| '''Scheme 14:''' Stabilized Carbanions are Planar and Achiral]]
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==Radicals and Stereochemistry==
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The same thing applies for radicals - we lose stereochemical intergrity when we form a radical from an enantiopure compound (if the radical is at the stereocentre).
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[[Image:Radicals Give Scrambling.png|thumb|center|400px| '''Scheme 15:''' Forming Radicals Destroys Stereochemical Integrity]]
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...because the intermediate radical is planar.
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[[Image:Planar Radical.png|thumb|center|400px| '''Scheme 16:''' Planarity of Radicals]]
==The Licence for This Page==
==The Licence for This Page==
Is [http://creativecommons.org/licenses/by/3.0/ CC-BY-3.0] meaning you can use whatever you want, provided you cite me.
Is [http://creativecommons.org/licenses/by/3.0/ CC-BY-3.0] meaning you can use whatever you want, provided you cite me.

Revision as of 08:38, 7 April 2013

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Contents

Chem3x11 Lecture 4

This is a general lecture on mechanisms, molecular orbitals and reactive intermediates.

(Back to the main teaching page)

Key concepts

  • Molecular orbitals impose geometrical restrictions on reaction mechanisms
  • The stereochemical outcome of a reaction can tell is a lot about a reaction mechanism
  • Intermediates like carbocations, carbanions and radicals can destroy the stereochemical integrity of enantiopure starting materials

Why do we Study Reaction Mechanisms?

A reaction mechanism is the detail of how/why one molecule becomes another. Why do we care? Three reasons:

1) Truth - even if a reaction is well-behaved, we're human being and like to understand the universe.

Scheme 1: A Well-behaved Organic Reaction
Scheme 1: A Well-behaved Organic Reaction

2) Complexity - in many cases reactions do unexpected things. Reactions never "don't work" - they either give back unreacted starting material, give the expected product, give something else, or give mixtures of things. Frequently we want to understand reaction mechanisms so we can understand complex reaction outcomes - the "Why did that happen?" question.

Scheme 2: A Reaction Giving Multiple Products
Scheme 2: A Reaction Giving Multiple Products

3) Prediction - if we understand reaction mechanisms we can start to make intelligent predictions about how to make new reactions work.

Scheme 3: A New Reaction for which we need to Predict Reagents and Conditions
Scheme 3: A New Reaction for which we need to Predict Reagents and Conditions

Stereochemistry is useful in the study of reaction mechanisms. If we compare the stereochemistry of starting materials with the stereochemistry in the products, we can deduce things that must have happened in a reaction mechanism even if we can't see those things directly. This forms one very useful part of the study of mechanisms (when coupled with things like spectroscopy and kinetics).

In this lecture we'll talk about the standard polar organic reactions that you've seen already.

Scheme 4: Polar Organic Reactions
Scheme 4: Polar Organic Reactions

The first thing to say, by way of introduction, is that we need to remember that reactions don't just happen as if by magic between the two ions. The nucleophile and electrophile have molecular orbitals on them that need to align for a reaction to occur. In the case of polar reactions an electron pair in a filled molecular orbital on the nucleophile needs to overlap with an empty molecular orbital on the electrophile. Good overlap (giving a strong bond) requires these orbitals be close in energy.

Scheme 5: Polar Organic Reactions
Scheme 5: Polar Organic Reactions

A good nucleophile tends to have a high energy Highest Occupied Molecular Orbital (HOMO) while a good electrophile tends to have a low energy Lowest Unoccupied Molecular Orbital (LUMO).

Mechanism of the SN2 Reaction Revisited

We all remember the SN2 reaction, where bond formation and breaking occurs in a single rate-limiting step. The HOMO in the examples below is the lone pair in an sp orbital on the hydroxide O, while the LUMO is the σ* orbital of the C-I bond.

Scheme 6: The SN2 Reation
Scheme 6: The SN2 Reation

Focussing on the frontier orbitals (the HOMOs and LUMOs) gives a reason for the inversion of stereochemistry that is observed when this reaction takes place.

Scheme 7: HOMO/LUMO Interactions in the SN2 Reaction
Scheme 7: HOMO/LUMO Interactions in the SN2 Reaction

Note that just based on the frontier orbitals, the nucleophile could in theory attack the iodine end of the molecule here, but the whole process is higher in energy.

Scheme 8: Energy Profile for the SN2 Reaction for both the Actual Reaction and an Alternative
Scheme 8: Energy Profile for the SN2 Reaction for both the Actual Reaction and an Alternative

And we can prove all this (backside attack and no intermediates) by using an enantiopure substrate - an SN2 reaction gives an enantiopure inverted product in the following sequence.

Scheme 9: Inversion of Configuration Observed in a Real SN2 Reaction
Scheme 9: Inversion of Configuration Observed in a Real SN2 Reaction

Mechanism of the SN1 Reaction Revisited

Some evidence for a planar (achiral) intermediate in the SN1 reaction comes from the scrambling of the stereochemistry.

Scheme 10: Generic SN1 Reaction with Mystery Intermediate
Scheme 10: Generic SN1 Reaction with Mystery Intermediate

The energy profile for this reaction includes an intermediate - i.e. a local energy minimum referring to a theoretically isolable species. The intermediate is the carbocation

Scheme 11: The SN1 Reaction Coordinate Diagram
Scheme 11: The SN1 Reaction Coordinate Diagram

When we consider factors that promote an SN1 reaction we are allowed to consider things that stabilise the carbocation. Note that this is an approximation - what we ought to be doing is considering things that stabilise the transition state leading to the carbocation. The Hammond Postulate tells us that because the carbocation is fairly high in energy compared to the species either side, the transition states will resemble the carbocation itself. What factors favour SN1 processes? Obvious things like polar solvents, adjacent π systems and adjacent lone pairs. Adjacent carbonyl groups do not - it turns out the only orbital that can interact with the carbocation is the C=O π* orbital, but since these are both empty there is no stabilization.

Carbanions and Stereochemistry

Take an enantiopure alkyl halide and make a Grignard out of it and you will be sorely disappointed in the enantiomeric excess of the product of your reaction with that Grignard.

Scheme 12: Formation of a Grignard Gives a Racemate in the Reaction Product
Scheme 12: Formation of a Grignard Gives a Racemate in the Reaction Product

Carbanions don't (usually) retain their stereochemical integrity, which is kind of annoying actually.

Scheme 13: Stereochemical Scrambling of a Grignard Reagent
Scheme 13: Stereochemical Scrambling of a Grignard Reagent

The same thing holds for many carbanions, particularly if the charge is somehow stabilized.

Scheme 14: Stabilized Carbanions are Planar and Achiral
Scheme 14: Stabilized Carbanions are Planar and Achiral

Radicals and Stereochemistry

The same thing applies for radicals - we lose stereochemical intergrity when we form a radical from an enantiopure compound (if the radical is at the stereocentre).

Scheme 15: Forming Radicals Destroys Stereochemical Integrity
Scheme 15: Forming Radicals Destroys Stereochemical Integrity

...because the intermediate radical is planar.

Scheme 16: Planarity of Radicals
Scheme 16: Planarity of Radicals

The Licence for This Page

Is CC-BY-3.0 meaning you can use whatever you want, provided you cite me.

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