What is reductive elimination in elimination reactions?
DISCLAIMER: You will NOT see this in first-semester inorganic chemistry.
This can be seen is in the elimination of two ligands from an octahedral metal-ligand complex, reducing the metal to a lower oxidation state.
In general, the reduction of the transition metal in an octahedral complex reduces the number of electrons around it by 2, from 18 to 16.
This is the opposite of oxidative addition. EXAMPLE 1 One example is the concerted reduction of
I've highlighted the ligands that leave the octahedral complex to form the new square planar complex. Afterwards, the chlorine, which was previously axial, has shifted to take the place of the now-missing equatorial methyl and becomes equatorial. Furthermore, this complex reduces from 18 to 16 electrons around the central metal. Since the Then, after the two hydrides leave, rhodium reduces to a EXAMPLE 2 Another example is the concerted reduction of
Notice how both of these concerted reductive elimination reactions required a cis relationship to the to-be-eliminated ligands. The acyl didn't leave with the chloride in the first reaction, nor did the hydride leave with the carbonyl in the second reaction. As before, this complex also reduces from 18 to 16 electrons around the central metal. Since the two Then, after the two hydrides leave, we gain a The mechanism for this seems to be the following:
I would not expect that the curved-arrow mechanism is known with good certainty, so don't feel like you have to figure out how to draw the mechanistic arrows.
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Reductive elimination is a step in elimination reactions where two substituents or functional groups are removed from adjacent atoms in a molecule to form a new bond, typically a double or triple bond. This process often occurs in transition metal catalyzed reactions, where a metal complex facilitates the removal of two ligands from a metal center to generate a new compound. Reductive elimination involves the simultaneous transfer of electrons and breaking of bonds, resulting in the formation of a new bond and the release of the eliminated groups as a product.
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When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
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