Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and...

32
Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not readily understood
  • date post

    21-Dec-2015
  • Category

    Documents

  • view

    217
  • download

    0

Transcript of Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and...

Page 1: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

Chem 125 Lecture 2210/27/08

This material is for the exclusive use of Chem 125 students at Yale and

may not be copied or distributed further.

It is not readily understood without reference to notes or the wiki from the lecture.

Page 2: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

1832

Radical Theory

Page 3: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

Oil of Bitter

Almonds

Page 4: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

Toward Structure With Analysis?

Oil ofBitter

Almonds

C7H6O2O2

C7H5OClCl2

Liebig & Wöhler (1832)

C7H6O

C7H5OBr

Br2

C7H5OIKI

C7H7ONNH3

C14H10O2S

PbS

So?Persistence of C7H5O Benzoyl Radical

Bz • H

Bz • OH

Bz • Cl

Bz • Br

Bz • I

Bz • NH2

Bz2 • S

Organic Dualism

A radical can be the “base” of more than just an acid!

Page 5: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

During the 1830s compound radicals were discovered

everywhere:Liebig: Acetyl

Bunsen: Cacodyl (Me2As •)

Piria: Salicyl

Dumas: Methyl Cetyl Cinnamyl Ethylene

Ethyl (Berzelius)

Page 6: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

e.g. Ethyl Chloride

-yl from (wood , matter)

ether from (to shine) 1700s

hence eth yl (Liebig, 1834)

Dualistic Radical Theory Survives

Two Words (+ and -)in our Nomenclature

sky

colorless liquid

Page 7: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

meth- from (wine, spirit)

-yl from (wood, matter)

-ene Greek Feminine

Patronymic"daughter of"

from

(1840) CH3 methyl from methylene

"Daughter of wood spirits"

hence meth yl ene (Dumas, 1835)

CH3OH = CH2 + H2O

(1852) ethylene C2H4

: ethyl :: methylene : methyl: C2H5 :: CH2 : CH3

Page 8: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

C3 C4

C3H7 PropylC3H6 Prop(yl)ene

C4H9 ButylC4H8 But(yl)ene

From C3 Propionic Acid (1847)

(protos first) (pion fat)Derivatives of acids with >C2 were like fats,

unlike C1 (formic) and C2 (acetic)

From C4 Butyric Acid (1826)

Lat. butyrum (butter)from rancid butter

Page 9: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

Jean-Baptiste

André Dumas

(7/14/1800-1884)Post-Napoleonic

Guardian ofFrench Chemistry

Persistent Opponentof Liebig and

Berzelius

Chaired Professor:Sorbonne 1841-

École Polytechnique 1835-École de Médicine 1839-

http

://c

lend

enin

g.ku

mc.

edu

Page 10: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

Note on the Present State of Organic Chemistry by MM. Dumas and Liebig (1837)

Sixty years have hardly passed since the ever memorable time when this same assembly heard the first discussions of the fertile chemical doctrine which we owe to the genius of Lavoisier. This short span of time has sufficed to examine fully the most delicate questions of inorganic chemistry, and anyone can easily convince himself that this branch of our knowledge possesses almost everything that it can with the methods of observation available.

…there barely remain a few cracks here and there to fill in.

MYOPIA!

(cf. Lavoisier, “in our own time”)

Page 11: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

In a word, how with the help of the laws of inorganic chemistry can one explain and classify such varied sub-stances as one obtains from organic bodies, and which nearly always are formed only of carbon, hydrogen, and oxygen, to which elements nitrogen is sometimes joined?

This was the great and beautiful question of natural philosophy,

prin

tart

ist

Note on the Present State of Organic Chemistry by MM. Dumas and Liebig (1837)

Page 12: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

Note on the Present State of Organic Chemistry by MM. Dumas and Liebig (1837)

a question well designed to excite the highest degree of competition among chemists; for once resolved the most beautiful triumphs were promised to science. The mysteries of plants, the mysteries of animal life would be unveiled before our eyes; we would seize the key to all the changes of matter, so sudden, so swift, so singular, that occur in animals and plants; more importantly we would find the means of duplicating them in our laboratories.

Page 13: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

Note on the Present State of Organic Chemistry by MM. Dumas and Liebig (1837)

Well, we are not afraid to say it, and it is not an asser-tion which we make lightly: this great and beautiful ques-tion is today answered; it only remains to follow through on all the consequences which its solution entails... In fact to produce with three or four elements such varied combinations, more varied perhaps than those which make up the whole inorganic kingdom, nature has chosen a path as simple as it was unexpected; for with elements she has made compounds which behave in all their properties like elements themselves. And this, we are convinced, is the entire secret of organic chemistry.

Page 14: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

Note on the Present State of Organic Chemistry by MM. Dumas and Liebig (1837)

Thus organic chemistry possesses its own elements, which sometimes play the role of chlorine or oxygen in inorganic chemistry and sometimes, on the contrary, play the role of metals. Cyanogen, amide, benzoyl, the radicals of ammonia, of aliphatics, of alcohol, and analogous substances, these are the true elements with which organic chemistry operates…

To discover these radicals, to study them, to characterize them, this has been our daily study for ten years.

+

Page 15: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

Note on the Present State of Organic Chemistry by MM. Dumas and Liebig (1837)

Sometimes, none the less, our opinions have appeared to differ, and then, with each of us drawn on by the heat of our battle with nature, there arose between usdiscussions whose liveliness we both regret.

Actually when we were able to discuss questions which separated us in several friendly meetings, we soon realized that we were in agreement on the principles...

We then understood that united we could undertake a task before which either of us in isolation would have recoiled…

We will analyze every organic substance…to establish reliably what sort of radical it refers to…

Page 16: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

Note on the Present State of Organic Chemistry by MM. Dumas and Liebig (1837)

Each of us has, in fact, opened his laboratory to all young men who were motivated by true love of science; they have seen all, understood all. We have worked under their eyes, and have had them work under ours, in such a way that we are surrounded by young rivals, who are the hope of science, and whose work will be added to ours

and mingle with ours, for it will have been conceived in the same spirit and carried out by the same methods…This is not an effort conceived for personal gain or in the interest of narrow vanity. No, and in a collaboration which is perhaps unheard of in the history of science, this is an undertaking in which we hope to interest every chemist in Europe. (unimaginative megalomania)

Page 17: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

Trouble in Paradise

C7H5O • H C7H5O • ClCl H • Cl+ = +C7H5O • Cl+ -

H • Cl+ -

The electronic character of radicals wastroublesome for Coulombic dualism.

++C7H5O • H

?

e.g. preparation of benzoyl chloride

Page 18: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

1840s - 1850s

Substitutionor Type or Unitary

Theory

Page 19: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

Tuileries

Bal costumé au Palais des Tuileries. 1867

organic compounds can

"fix" chlorine gas!

Violently irritating fumes from wax

candles spoil soiréeat the Tuileries Palace (~1830)

Dumas identifies the culprit as HCl from wax that had

been bleached by Cl2.

Mus

ée d

'Ors

ay (

ww

w.h

isto

ire-

imag

e.or

g)

cough!choke!

Page 20: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

Two ways wax could "fix" chlorine:

Cl Cl*

C

CH2

H2

+*+

Addition of Cl2 to an Alkene (HOMO/LUMO)

ClC

CCl

H2

H2

C

C

H2

H2Cl

Cl

(actually both steps at once)

Cln

••

••

••

HOMOLUMO LUMOHOMO

HOMO / LUMO

“olefiant gas” “oil of Dutch chemists” (1795)

Page 21: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

Free-Radical Substitution of Cl for H (SOMO)• •

Two ways wax could "fix" chlorine:

H CH3Cl Clweak bond

(58 kcal/mole)

••

SOMO

H Cl

CH3 Cl Cl

CH3Cl

Cl

single-electrons

single-barbedarrows

"free-radical chain"

Cl ClC

CH2

H2

+

Addition of Cl2 to an Alkene (HOMO/LUMO)

ClC

CCl

H2

H2

C

C

H2

H2Cl

Cl

No high HOMO!“make-as-you-break”

“make-as-you-break”

Still hard to break!

Use light to promote an electron to *Cl-Cl

lots of product from one initial photolysis

Page 22: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

1830s - 1850s

“Substitution”or “Type”

or “Unitary”Theory

Page 23: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

C2H3O • OH C2H2ClO • OH

Photochlorination of acetic acidtransmuted the acetyl "element".

Cl H • Cl+ = +C2H3O • OH C2H2ClO • OH

More Trouble for Radicals - Dumas (1839)

Hydrogen may be substituted by anequivalent amount of halogen, oxygen, etc.

Similar Acids! C2HCl2O • OH

C2Cl3O • OH

without changing molecular type.

Page 24: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

Four Types Recognized by 1853

H

H

H

Cl

H

HO

H

HN H

C2H5

HO

C2H5

HN H

KC2H5

C2H5

C2H5

I+ =

C2H5

C2H5

O + KI

Williamson Ether Synthesis (1850)

Page 25: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

Butyl_BromideTwo-Word Relic

of Radical Dualism

BromobutaneOne-Word Relic

of "Unitary" Theory

Unitary (not Dualistic) Theory [Molecules are like] planetary systems held together by a force resembling gravitation, but acting in accord with much more complicated laws. Dumas (1840)

Formulae…may be used as an actual image of what we rationally suppose to be the arrangement of constituent atoms in a compound, as a orrery is an image of what we conclude to be the arrangement of our planetary system. A. W. Williamson (age 27, 1851)

A Philosopher lecturing on the Orrery Joseph Wright of Derby (1766)

Page 26: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

A neutral anhydrous tartrate loses an atom of water at +190°; it has ceased to be a tartrate and has become another salt

Berzelius (1838)

“By reacting chlorine with ordinary ether [Dumas] pro-duced a very interesting compound which he reckoned, according to the theory of substitutions, to be an ether in which 4 atoms of chlorine replace 4 atoms of hydrogen. An element as eminently electronegative as chlorine would never be able to enter into an organic radical : this idea is contrary to the first principles of chemistry…”

first use of “R” to denote a generalized radical

Page 27: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

“Liebig’s Annalen”

I am a far cry from sharing the ideas that M. Dumas

has linked to the so-called laws of

the substitution theory.

1840

On the Reaction of Chlorine with the Chlorides of Ethanol

and Methanol and Several Points of the Ether Theory.

On the Substitution Lawof M. Dumas.

Remarks on the Previous Paper

Can one substitute the elements that play their role in any

simple or compound substance equivalent for equivalent ?

On the Law of Substitutions andthe Theory of Types.

Justus Liebig

*) Letter to J.L.

On the Law of Substitutions andthe Theory of Types.*

YES!

Page 28: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

On the Substitution Law and the Theory of Types

(letter to Justus Liebig) Paris, 1 March 1840

Monsieur! I am eager to communicate to you one of the most striking facts of organic chemistry. I have confirmed the substitution theory in an extremely remarkable and completely unexpected manner. Only now can one appreciate the great value of this theory and foresee the immense discoveries that it promises to reveal.

manganese acetate [MnO + C4H6O3]

[Cl2Cl2 + Cl8Cl6Cl6]

[MnCl2 + C4Cl6O3]

[Cl2Cl2 + C4Cl6O3]

[MnO + C4Cl6O3]

Page 29: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

On the Substitution Law and the Theory of Types

(letter to Justus Liebig)

For all I know, in the decolorizing action of chlorine, hydrogen is replaced by chlorine, and the cloth, which is now being bleached in England, preserves its type accor-ding to the substitution laws.* I believe, however, that atom-for-atom substitution of carbon by chlorine is my own discovery. I hope you will take note of this in your journal and be assured of my sincerest regards, etc.

S. C. H. Windler

* I have just learned that there is already in the London shops a cloth of chlorine thread, which is very much sought after and preferred above all others for night caps, underwear, etc.

*

Page 30: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

In 1849 Kolbe Prepared Free Methyl Radical

(electrolysis)

CH3 • CO2H CH3 CO2 H+ +

but molecular weight would showhe had its dimer H3C-CH3

(Cannizzaro, 1860)

Page 31: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

CO

HC

O

OH

O2

CO

OHC

O

OH

Cl2H3C CH2Cl

CO

OCH3

-e-

H3C CH3-CH3•

Ironically the key reactions of both radical and type theories did involve free radicals

(SOMO not HOMO/LUMO)

CO

CO

OHH2C

Page 32: Chem 125 Lecture 22 10/27/08 This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further. It is not.

End of Lecture 22Oct. 27, 2008