---
title: "Organometallic Catalysis: Elementary Steps and Cycles"
book: "University Chemistry — Year 2"
subject: chemistry
language: en
chapter: 20
exercises: 12
source: https://one-course.com/books/chemistry/3/en/chapter/20-organometallic-catalysis-elementary-steps-and-cycles
license: CC-BY-NC-SA-4.0
credit: "One Chemistry Book, One Course (one-course.com)"
---

# Chapter 20 — Organometallic Catalysis: Elementary Steps and Cycles

A few milligrams of a palladium salt can join two [aromatic](https://one-course.com/books/chemistry/3/en/chapter/16-huckel-theory-and-conjugated-systems#def-b2-huckel-aromatic) rings in a flask holding kilograms of reagents: the same metal atom does the job thousands of times, coming back to its starting state after each pass. How it does so is told by a [catalytic cycle](#def-b2-catalytic-cycles-cycle), a closed sequence of a handful of elementary steps. There are only a few kinds of step, and each changes the oxidation state, the electron count and the number of ligands of the metal in a fixed way. With the electron count of [Chapter 18](https://one-course.com/books/chemistry/3/en/chapter/18-transition-metals-and-coordination-complexes#ch-b2-coordination-complexes), a cycle can be read, checked, and sometimes predicted.

**You already know.**

[Chapter 18](https://one-course.com/books/chemistry/3/en/chapter/18-transition-metals-and-coordination-complexes#ch-b2-coordination-complexes): oxidation state, $d^n$, [valence electron count](https://one-course.com/books/chemistry/3/en/chapter/18-transition-metals-and-coordination-complexes#def-b2-coordination-complexes-electron-count), [18-electron rule](https://one-course.com/books/chemistry/3/en/chapter/18-transition-metals-and-coordination-complexes#def-b2-coordination-complexes-electron-count), [hapticity](https://one-course.com/books/chemistry/3/en/chapter/18-transition-metals-and-coordination-complexes#def-b2-coordination-complexes-hapticity). [Chapter 19](https://one-course.com/books/chemistry/3/en/chapter/19-ligand-field-theory-and-colour#ch-b2-ligand-field): $\pi$-acceptor ligands and [back-donation](https://one-course.com/books/chemistry/3/en/chapter/19-ligand-field-theory-and-colour#def-b2-ligand-field-pi-ligands). The Year 1 volume: catalyst, homogeneous catalysis, elementary step, rate-determining step, organometallic compound, oxidation number.

![A pilot plant of process chemistry: a glass-lined steel reactor, where a catalysed coupling is scaled up from the flask before production.](https://one-course.com/images/onecourse/chapters/chemistry-3/b2-catalytic-cycles/img-c0661cffae9d.jpg)

*A pilot plant of process chemistry: a glass-lined steel reactor, where a catalysed coupling is scaled up from the flask before production.*

## 20.1 The language of organometallic complexes

Organometallic complexes are counted as in [Method 18.11](https://one-course.com/books/chemistry/3/en/chapter/18-transition-metals-and-coordination-complexes#met-b2-coordination-complexes-electron-count), with a few more ligands: a hydride $\ce{H-}$ and an alkyl or aryl anion $\ce{R-}$ give two electrons each and count $-1$ in the oxidation state; $\ce{CO}$, phosphines $\ce{PR3}$ and $\eta^2$-alkenes give two electrons and count 0; a halide $\ce{X-}$ gives two and counts $-1$.

**Definition 20.1 (Unsaturated complexes).**

A *coordinatively unsaturated complex* has fewer than 18 valence electrons (often 16) and can bind another ligand: it has a *vacant site*, a position of its [coordination sphere](https://one-course.com/books/chemistry/3/en/chapter/18-transition-metals-and-coordination-complexes#def-b2-coordination-complexes-coordination-sphere) free to receive a two-electron donor.

Square-planar $d^8$ complexes of rhodium(I), iridium(I), palladium(II) and platinum(II) are 16-electron complexes; palladium(0) bisphosphines $\ce{PdL2}$ have 14. Such complexes are the active species of most [catalytic cycles](#def-b2-catalytic-cycles-cycle).

**Method 20.2 (Counting an organometallic complex).**

1. List the ligands: anionic ( $\ce{H-}$ , $\ce{R-}$ , $\ce{X-}$ , $\ce{C5H5-}$ ) and neutral ( $\ce{CO}$ , $\ce{PR3}$ , alkenes, solvent).
2. Oxidation state = charge of the complex $-$ sum of the anionic ligand charges.
3. $n = g -$ oxidation state; count = $n + 2 \times$ (number of two-electron donors) $+$ 6 per $\eta^5$ - $\ce{C5H5-}$ .
4. Coordination number = number of ligand positions occupied.

## 20.2 Ligand exchange, oxidative addition, reductive elimination

**Definition 20.3 (Ligand exchange).**

A *ligand exchange* is an elementary step in which a ligand of the [coordination sphere](https://one-course.com/books/chemistry/3/en/chapter/18-transition-metals-and-coordination-complexes#def-b2-coordination-complexes-coordination-sphere) is replaced by another; it changes neither the oxidation state nor, overall, the electron count. Its mechanisms are studied in the Year 3 volume.

**Definition 20.4 (Oxidative addition and reductive elimination).**

In an *oxidative addition*, a molecule A–B adds to a metal centre by breaking its A–B bond and forming M–A and M–B bonds. A *reductive elimination* is the reverse step: two ligands A and B, cis to each other, join into A–B and leave the metal.

**Proposition 20.5 (Counting an oxidative addition).**

An [oxidative addition](#def-b2-catalytic-cycles-oxidative-addition) raises the oxidation state of the metal by 2, its [valence electron count](https://one-course.com/books/chemistry/3/en/chapter/18-transition-metals-and-coordination-complexes#def-b2-coordination-complexes-electron-count) by 2 and its coordination number by 2; a [reductive elimination](#def-b2-catalytic-cycles-oxidative-addition) lowers each by 2.

**Proof.** A and B are counted as anions ($\ce{H-}$, $\ce{R-}$, $\ce{X-}$) once bound: two new anionic ligands raise the oxidation state by 2 and lower $n$ by 2; they give two pairs, $+4$ electrons; the count changes by $-2 + 4 = +2$. Two positions are newly occupied. The reverse step reverses every change. ∎

**Example 20.6 (Vaska’s complex).**

$\ce{[IrCl(CO)(PPh3)2]}$, square planar: iridium(I), $d^8$, 16 electrons, four-coordinate. It adds dihydrogen: $\ce{[IrH2Cl(CO)(PPh3)2]}$, iridium(III), $d^6$, 18 electrons, octahedral, the two hydrides cis.

## 20.3 Insertion, elimination, transmetalation

**Definition 20.7 (Insertion and β\betaβ-hydride elimination).**

In a *migratory insertion*, an unsaturated ligand (alkene, $\ce{CO}$) bound to the metal inserts into a cis M–H or M–C bond: $\ce{M-H}$ and an alkene give an alkyl $\ce{M-CH2-CH2-H}$; $\ce{M-R}$ and $\ce{CO}$ give an acyl $\ce{M-C(=O)R}$. A *$\beta$-hydride elimination* is the reverse of an alkene insertion: a hydrogen on the carbon $\beta$ to the metal moves onto the metal, releasing an alkene.

**Proposition 20.8 (Counting an insertion).**

A [migratory insertion](#def-b2-catalytic-cycles-insertion) keeps the oxidation state and lowers the electron count by 2 (one ligand position is freed); a $\beta$-hydride elimination raises the count by 2.

**Proof.** Before: $\ce{H-}$ (or $\ce{R-}$, anionic) and the alkene (neutral), two ligands, four electrons. After: one alkyl (anionic), two electrons. The anionic charge is unchanged: same oxidation state; two electrons and one position lost. ∎

**Proposition 20.9 (Conditions for β\betaβ-hydride elimination).**

A metal alkyl undergoes $\beta$-hydride elimination only if the alkyl carries a hydrogen on its $\beta$ carbon and the metal has a [vacant site](#def-b2-catalytic-cycles-unsaturated) cis to the alkyl.

**Argument.** The step goes through a four-membered arrangement M–C$_\alpha$–C$_\beta$–H in which the hydrogen reaches the metal: it needs that hydrogen, and an empty position next to the alkyl to receive it. Methyl, benzyl, neopentyl and aryl groups, which have no $\beta$ hydrogen able to reach the metal, are stable towards it. ∎

**Definition 20.10 (Transmetalation).**

A *transmetalation* transfers an organic group from one metal (or metalloid: boron, zinc, tin) to another, usually in exchange for a halide.

![The elementary steps of organometallic catalysis. Oxidative addition: oxidation state, count and coordination number +2; reductive elimination: -2. Migratory insertion: count -2, oxidation state unchanged; -hydride elimination: the reverse. Transmetalation: an organic group moves to the metal from boron, zinc or tin.](https://one-course.com/images/onecourse/chapters/chemistry-3/b2-catalytic-cycles/fig-e3597d53fad8.svg)

*The elementary steps of organometallic catalysis. [Oxidative addition](#def-b2-catalytic-cycles-oxidative-addition): oxidation state, count and coordination number $+2$; [reductive elimination](#def-b2-catalytic-cycles-oxidative-addition): $-2$. [Migratory insertion](#def-b2-catalytic-cycles-insertion): count $-2$, oxidation state unchanged; $\beta$-hydride elimination: the reverse. [Transmetalation](#def-b2-catalytic-cycles-transmetalation): an organic group moves to the metal from boron, zinc or tin.*

## 20.4 Reading a catalytic cycle

**Definition 20.11 (Catalytic cycle).**

A *catalytic cycle* is a closed sequence of elementary steps that consumes the reagents, releases the products and regenerates its first complex. The compound added to the reaction, which turns into the first complex of the cycle, is the *precatalyst*. The *turnover number* (TON) is the amount of product formed per amount of catalyst; the *turnover frequency* (TOF) is the turnover number per unit time.

**Proposition 20.12 (The overall equation).**

The sum of the steps of a [catalytic cycle](#def-b2-catalytic-cycles-cycle) is the equation of the catalysed reaction: every metal complex appears once as a product and once as a reactant, and cancels.

**Proof.** The cycle being closed, each intermediate is formed by one step and consumed by the next; adding the steps, these species appear on both sides and cancel. What remains are the species that enter from outside (reagents) and leave (products). ∎

**Method 20.13 (Reading a cycle).**

1. For each complex, compute the oxidation state, the electron count and the coordination number.
2. Name each step from the changes ( $+2/+2/+2$ : [oxidative addition](#def-b2-catalytic-cycles-oxidative-addition) ; count $-2$ at constant oxidation state: insertion; and so on).
3. Check that no complex exceeds 18 electrons and that a step needing a [vacant site](#def-b2-catalytic-cycles-unsaturated) starts from an unsaturated complex.
4. Add the steps: the sum must be the overall equation.

![The hydrogenation of an alkene with Wilkinson’s catalyst, simplified (phosphine and solvent exchanges omitted). The four steps sum to RCH=CH2 + H2 -> RCH2CH3; the rhodium complexes cancel.](https://one-course.com/images/onecourse/chapters/chemistry-3/b2-catalytic-cycles/fig-59c4244ae108.svg)

*The hydrogenation of an alkene with Wilkinson’s catalyst, simplified (phosphine and solvent exchanges omitted). The four steps sum to $\ce{RCH=CH2 + H2 -> RCH2CH3}$; the rhodium complexes cancel.*

![The Suzuki coupling, simplified. Palladium(0) adds the aryl bromide; the base turns the boronic acid into a borate, which transfers its aryl group to palladium; the two aryls, cis, are eliminated as the biaryl, regenerating palladium(0).](https://one-course.com/images/onecourse/chapters/chemistry-3/b2-catalytic-cycles/fig-d86f26c55a43.svg)

*The Suzuki coupling, simplified. Palladium(0) adds the aryl bromide; the base turns the boronic acid into a borate, which transfers its aryl group to palladium; the two aryls, cis, are eliminated as the biaryl, regenerating palladium(0).*

In the Heck reaction, the aryl–palladium complex formed by [oxidative addition](#def-b2-catalytic-cycles-oxidative-addition) binds an alkene instead of a borate; [migratory insertion](#def-b2-catalytic-cycles-insertion) puts the aryl on the alkene, and a $\beta$-hydride elimination releases the substituted alkene (usually the trans isomer) and a palladium hydride, from which a base removes $\ce{HBr}$ to regenerate palladium(0).

Hydroformylation, the addition of $\ce{H2}$ and $\ce{CO}$ across an alkene to give an aldehyde, runs on cobalt or rhodium hydrides through insertion of the alkene, insertion of $\ce{CO}$ into the metal–alkyl bond, [oxidative addition](#def-b2-catalytic-cycles-oxidative-addition) of $\ce{H2}$ and [reductive elimination](#def-b2-catalytic-cycles-oxidative-addition) of the aldehyde. The direction of the first insertion decides the product: the metal on the terminal carbon gives the linear aldehyde, on the inner carbon the branched one; bulky phosphines favour the linear product.

**History — Cross-coupling.**

![](https://one-course.com/images/onecourse/chapters/chemistry-3/b2-catalytic-cycles/img-f2b80b04598b.jpg)

Palladium-catalysed couplings of aryl and vinyl halides with alkenes (Richard Heck, from 1968), with organozinc reagents (Ei-ichi Negishi, 1977) and with organoboron compounds (Akira Suzuki, 1979) made the joining of two carbon frameworks routine; they are now among the most used reactions in the making of medicines and materials. The Nobel Prize in Chemistry was awarded to the three in 2010. (Photograph: Suzuki, Negishi and Heck, left to right, 2010; BloodIce, CC BY-SA 4.0, Wikimedia Commons.)

**Proposition 20.14 (Turnover).**

With $n_P$ the amount of product formed in a time $t$ by an amount $n_{\text{cat}}$ of catalyst, $\mathrm{TON} = n_P/n_{\text{cat}}$ and the mean [turnover frequency](#def-b2-catalytic-cycles-cycle) is $\mathrm{TOF} =
\mathrm{TON}/t$.

**Proof.** Each turn of the cycle makes one product molecule per metal atom; the number of turns made by each atom on average is $n_P/n_{\text{cat}}$, and the rate of turning is that number per unit time. ∎

**Safety.**

![](https://one-course.com/images/onecourse/chapters/chemistry-3/b2-catalytic-cycles/fig-afc03563fb34.svg)

![](https://one-course.com/images/onecourse/chapters/chemistry-3/b2-catalytic-cycles/fig-b3bf7bb196be.svg)

![](https://one-course.com/images/onecourse/chapters/chemistry-3/b2-catalytic-cycles/fig-76745c6dd418.svg)

Palladium(II) ethanoate is corrosive to the eyes and toxic to aquatic life; triphenylphosphine is harmful and a sensitiser. They are weighed in a fume hood, and the palladium residues are collected for recovery, never poured down the drain.

## 20.5 Exercises

**Exercise 20.1 ★.**

Give the oxidation state, $d^n$ and electron count of Vaska’s complex $\ce{[IrCl(CO)(PPh3)2]}$ before and after it adds $\ce{H2}$.

**Solution of Exercise 20.1.**

Before: Ir(I), $d^8$, $8 + 4 \times 2 = 16$ electrons. After: Ir(III), $d^6$, $6 + 6 \times 2 = 18$ electrons, octahedral.

**Exercise 20.2 ★.**

Name the step: $\ce{[PtCl2(CH3)2(PR3)2] -> [PtCl2(PR3)2] + C2H6}$; $\ce{[Pd(Ph)Br(PR3)2] +
CH2=CH2 -> [Pd(CH2CH2Ph)Br(PR3)] + PR3}$.

**Solution of Exercise 20.2.**

The first is a [reductive elimination](#def-b2-catalytic-cycles-oxidative-addition) (Pt(IV) to Pt(II), ethane formed from two methyls). The second is a [ligand exchange](#def-b2-catalytic-cycles-ligand-exchange) (one phosphine replaced by ethene) followed by a [migratory insertion](#def-b2-catalytic-cycles-insertion) of ethene into the Pd–Ph bond.

**Exercise 20.3 ★.**

A reaction uses $0.020\,\mathrm{mmol}$ of catalyst and gives $15.0\,\mathrm{mmol}$ of product in $3.0\,\mathrm{h}$. Compute the TON and the mean TOF.

**Solution of Exercise 20.3.**

TON $= 15.0/0.020 = 750$; TOF $= 750/3.0 = 250\,\mathrm{h}^{-1}$.

**Exercise 20.4 ★.**

Add the three steps of the Suzuki cycle and check that palladium cancels.

**Solution of Exercise 20.4.**

$$
\begin{align*}
  &\mathrm{PdL_2 + ArBr \to ArPdBrL_2}\\
  &\mathrm{ArPdBrL_2 + Ar'B(OH)_3^- \to ArPdAr'L_2 + Br^- + B(OH)_3}\\
  &\mathrm{ArPdAr'L_2 \to Ar{-}Ar' + PdL_2}
\end{align*}
$$

Sum: $\mathrm{ArBr + Ar'B(OH)_3^- \to Ar{-}Ar' + Br^- + B(OH)_3}$; every palladium species cancels.

**Exercise 20.5 ★★.**

Which of these alkyl palladium complexes can undergo $\beta$-hydride elimination: $\ce{Pd-CH3}$, $\ce{Pd-CH2CH3}$, $\ce{Pd-CH2C(CH3)3}$, $\ce{Pd-CH2Ph}$, $\ce{Pd-CH(CH3)2}$?

**Solution of Exercise 20.5.**

Ethyl and isopropyl (they have $\beta$ hydrogens). Methyl has no $\beta$ carbon; neopentyl’s $\beta$ carbon carries no hydrogen; benzyl’s $\beta$ carbon is an [aromatic](https://one-course.com/books/chemistry/3/en/chapter/16-huckel-theory-and-conjugated-systems#def-b2-huckel-aromatic) ring carbon that carries no hydrogen.

**Exercise 20.6 ★★.**

Predict the product of the Heck reaction of iodobenzene with methyl propenoate, and its geometry.

**Solution of Exercise 20.6.**

Methyl (*E*)-3-phenylpropenoate, $\ce{Ph-CH=CH-COOCH3}$, the phenyl added to the terminal carbon, trans product.

**Exercise 20.7 ★★.**

Write the linear and branched aldehydes formed by the hydroformylation of propene, and explain which insertion leads to each.

**Solution of Exercise 20.7.**

Butanal $\ce{CH3CH2CH2CHO}$ (linear: the metal adds to the terminal carbon, the hydride to the inner one) and 2-methylpropanal $\ce{(CH3)2CHCHO}$ (branched: the metal on the inner carbon).

**Exercise 20.8 ★★.**

Why can $\ce{[RhCl(PPh3)3]}$ add $\ce{H2}$ only after losing a phosphine, while $\ce{[RhCl(PPh3)2]}$ adds it at once?

**Solution of Exercise 20.8.**

$\ce{[RhCl(PPh3)3]}$ has 16 electrons: adding $\ce{H2}$ (+2) would give 18 with six coordination positions, too crowded with three bulky phosphines. $\ce{[RhCl(PPh3)2]}$ has 14 and an open site: [oxidative addition](#def-b2-catalytic-cycles-oxidative-addition) gives a 16-electron complex easily.

**Exercise 20.9 ★★.**

In the Suzuki coupling, why is a base needed, and what does it do to the boronic acid?

**Solution of Exercise 20.9.**

The boronic acid is a poor nucleophile; the base adds hydroxide (or alkoxide) to boron, giving a borate $\ce{ArB(OH)3-}$, whose aryl group is more electron-rich and transfers to palladium.

**Exercise 20.10 ★★★.**

A proposed cycle for the hydrogenation of an alkene on a $d^8$ complex $\ce{ML3X}$ (16 e) starts with the binding of the alkene to give a 20-electron complex, then [oxidative addition](#def-b2-catalytic-cycles-oxidative-addition) of $\ce{H2}$. Find the error and correct the order.

**Solution of Exercise 20.10.**

A 20-electron complex is not reasonable. The complex must first lose a ligand (14 e), then add $\ce{H2}$ (16 e), bind the alkene (18 e), insert it into an M–H bond (16 e) and eliminate the alkane (14 e), before taking the ligand back or starting again.

**Exercise 20.11 ★★★.**

The amount of product of a catalysed reaction grows as $n_P(t) = n_{\max}(1 - \mathrm e^{-t/\tau})$ with $n_{\max} = 10.0\,\mathrm{mmol}$, $\tau = 40\,\mathrm{min}$ and $0.010\,\mathrm{mmol}$ of catalyst (exercise data). Compute the initial TOF and the final TON.

**Solution of Exercise 20.11.**

Initial rate $n_{\max}/\tau = 0.25\,\mathrm{mmol}/\mathrm{min}$; initial TOF $= 0.25/0.010 =
25\,\mathrm{min}^{-1} = 1.5 \times 10^{3}\,\mathrm{h}^{-1}$. Final TON $= 10.0/0.010 = 1.0 \times 10^3$.

**Exercise 20.12 ★★★.**

Propose a cross-coupling to prepare 4-methoxybiphenyl, choosing the halide and the boronic acid, and write the cycle.

**Solution of Exercise 20.12.**

4-Bromoanisole with phenylboronic acid (or bromobenzene with 4-methoxyphenylboronic acid), a palladium(0) phosphine catalyst and a base. Cycle: [oxidative addition](#def-b2-catalytic-cycles-oxidative-addition) of the aryl bromide, [transmetalation](#def-b2-catalytic-cycles-transmetalation) from the borate, [reductive elimination](#def-b2-catalytic-cycles-oxidative-addition) of 4-methoxybiphenyl.

## 20.6 Problem: Reading the Suzuki Cycle

**Problem 20.1.**

Weekend problem — the precatalyst and the active palladium(0), the oxidative addition, transmetalation and reductive elimination of a Suzuki coupling, the yield and the turnover number, and the side reactions

Run (exercise data): $10.0\,\mathrm{mmol}$ of 4-bromotoluene, $12.0\,\mathrm{mmol}$ of phenylboronic acid, $20\,\mathrm{mmol}$ of potassium carbonate, $0.050\,\mathrm{mmol}$ of palladium(II) ethanoate and $0.10\,\mathrm{mmol}$ of triphenylphosphine in a mixture of toluene, ethanol and water, heated under nitrogen; isolated product: $1.51\,\mathrm{g}$ of 4-methylbiphenyl. Molar masses ($\mathrm{g}/\mathrm{mol}$): 4-bromotoluene 171.04, phenylboronic acid 121.93, 4-methylbiphenyl 168.24, palladium(II) ethanoate 224.51.

**Part I — The catalyst.**

1. Give the oxidation state and $d^n$ of palladium in palladium(II) ethanoate.
2. In the flask it is reduced to $\ce{Pd(PPh3)2}$ . Give its oxidation state, $d^n$ and electron count.
3. Why is that complex coordinatively unsaturated?
4. Why is the reaction run under nitrogen?
5. What is the role of the excess triphenylphosphine?
6. Is palladium(II) ethanoate the catalyst or the [precatalyst](#def-b2-catalytic-cycles-cycle) ?

**Part II — The steps.**

7. Write the [oxidative addition](#def-b2-catalytic-cycles-oxidative-addition) of 4-bromotoluene and count the product.
8. What does the carbonate do to phenylboronic acid?
9. Write the [transmetalation](#def-b2-catalytic-cycles-transmetalation) .
10. Why must the two aryl groups be cis before the next step?
11. Write the [reductive elimination](#def-b2-catalytic-cycles-oxidative-addition) and count the palladium species formed.
12. Add the three steps.

**Part III — Yield and turnover.**

13. Which reagent is limiting?
14. Compute the amount of product isolated.
15. Compute the yield.
16. Compute the catalyst loading in mol % relative to the bromide.
17. Compute the [turnover number](#def-b2-catalytic-cycles-cycle) of palladium.
18. The run took $4.0\,\mathrm{h}$ . Compute the mean [turnover frequency](#def-b2-catalytic-cycles-cycle) per hour.

**Part IV — Side reactions.**

19. Some biphenyl $\ce{Ph-Ph}$ is found. Suggest how it forms.
20. Why is no $\beta$ -hydride elimination possible here?
21. An aryl chloride reacts much more slowly than the bromide. Which step suffers?
22. What happens to the palladium at the end of the reaction, and why is it recovered?
23. Why is a small excess of boronic acid used?
24. State the [turnover number](#def-b2-catalytic-cycles-cycle) of palladium in the run.

**Solution of Problem 20.1.**

**1.** Pd(II), $d^8$. **2.** Pd(0), $d^{10}$, $10 + 2 \times 2 = 14$ electrons. **3.** With 14 electrons it can accept two more pairs: it has [vacant sites](#def-b2-catalytic-cycles-unsaturated). **4.** Palladium(0) phosphine complexes are oxidised by air, and phosphines are oxidised to phosphine oxides. **5.** It reduces palladium(II) to palladium(0) (being oxidised itself) and binds the palladium(0), keeping it in solution. **6.** The [precatalyst](#def-b2-catalytic-cycles-cycle). **7.** $\ce{Pd(PPh3)2 + CH3C6H4Br -> [Pd(C6H4CH3)Br(PPh3)2]}$: Pd(II), $d^8$, $8 + 4 \times 2 =
16$ electrons. **8.** It turns it into the borate $\ce{PhB(OH)3-}$, which transfers its phenyl group. **9.** $\ce{[Pd(Ar)Br(PPh3)2] + PhB(OH)3- -> [Pd(Ar)(Ph)(PPh3)2] + Br- + B(OH)3}$. **10.** [Reductive elimination](#def-b2-catalytic-cycles-oxidative-addition) joins two cis ligands; trans aryls must first isomerise. **11.** $\ce{[Pd(Ar)(Ph)(PPh3)2] -> Ar-Ph + Pd(PPh3)2}$: palladium(0), 14 electrons, ready for another turn. **12.** $\ce{CH3C6H4Br + PhB(OH)3- -> CH3C6H4-Ph + Br- + B(OH)3}$. **13.** 4-Bromotoluene ($10.0\,\mathrm{mmol}$, against $12.0\,\mathrm{mmol}$ of boronic acid). **14.** $1.51/168.24 = 8.98 \times 10^{-3}\,\mathrm{mol}$, $8.98\,\mathrm{mmol}$. **15.** $8.98/10.0 = 89.8~\%$. **16.** $0.050/10.0 = 0.50$ mol %. **17.** $8.98/0.050 = 180$. **18.** $180/4.0 = 45\,\mathrm{h}^{-1}$. **19.** Two phenyl groups transferred to the same palladium (homocoupling of the boronic acid, favoured by traces of oxygen), then eliminated together. **20.** The aryl groups have no $\beta$ hydrogen able to reach the metal. **21.** The [oxidative addition](#def-b2-catalytic-cycles-oxidative-addition): the $\ce{C-Cl}$ bond is stronger than $\ce{C-Br}$. **22.** It ends as palladium(0) particles or salts in the residues; it is expensive and toxic, and is recovered. **23.** Part of the boronic acid is lost to side reactions (homocoupling, loss of boron from the ring); the excess keeps the bromide limiting. **24.** The palladium turned over $\boldsymbol{\approx 1.8 \times 10^{2}}$ times.