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Kekulé and .
Benzene, C < sub > 6 </ sub > H < sub > 6 </ sub >, is the simplest aromatic hydrocarbon and was recognized as the first aromatic hydrocarbon, with the nature of its bonding first being recognized by Friedrich August Kekulé von Stradonitz in the 19th century.
His rejection of structural chemistry, especially the theories of the structure of benzene by August Kekulé, the theory of the asymmetric carbon atom by J. H.
Friedrich August Kekule von Stradonitz ( also August Kekulé ; ) ( 7 September 1829 – 13 July 1896 ) was a German organic chemist.
Kekulé never used his first given name ; he was known throughout his life as August Kekulé.
Kekulé was born in Darmstadt, the son of a civil servant.
In 1856 Kekulé became Privatdozent at the University of Heidelberg.
This theory proceeds from the idea of atomic valence, especially the tetravalence of carbon ( which Kekulé announced late in 1857 ) and the ability of carbon atoms to link to each other ( announced in a paper published in May 1858 ), to the determination of the bonding order of all of the atoms in a molecule.
Among those who were most active in pursuing early structural investigations were, in addition to Kekulé and Couper, Frankland, Wurtz, Alexander Crum Brown, Emil Erlenmeyer, and Aleksandr Mikhailovich Butlerov.
In 1865 Kekulé published a paper in French ( for he was then still in Francophone Belgium ) suggesting that the structure contained a six-membered ring of carbon atoms with alternating single and double bonds.
Kekulé argued for his proposed structure by considering the number of isomers observed for derivatives of benzene.
For diderivatives such as the toluidines, C < sub > 6 </ sub > H < sub > 4 </ sub >( NH < sub > 2 </ sub >)( CH < sub > 3 </ sub >), three isomers were observed, for which Kekulé proposed structures with the two substituted carbon atoms separated by one, two and three carbon-carbon bonds, later named ortho, meta and para isomers respectively.
The counting of possible isomers for diderivatives was however criticized by Albert Ladenburg, a former student of Kekulé, who argued that Kekulé's 1865 structure implied two distinct " ortho " structures, depending on whether the substituted carbons are separated by a single or a double bond.
Friedrich August Kekulé von StradonitzThe need for an international standard for chemistry was first addressed in 1860 by a committee headed by German scientist Friedrich August Kekulé von Stradonitz.
The crucial breakthrough for organic chemistry was the concept of chemical structure, developed independently and simultaneously by Friedrich August Kekulé and Archibald Scott Couper in 1858.
The most important example is benzene, the structure of which was formulated by Kekulé who first proposed the delocalization or resonance principle for explaining its structure.
* 1829 – Friedrich August Kekulé von Stradonitz, German chemist ( d. 1896 )
* September 7 – Friedrich August Kekulé von Stradonitz, German chemist ( d. 1896 )

Kekulé and Couper
Couper adopted the atomic weight of oxygen as 8 rather than 16, so there are twice as many oxygen atoms in Couper's formulas as in those of Kekulé.

Kekulé and on
Basing his ideas on those of predecessors such as Williamson, Edward Frankland, William Odling, Auguste Laurent, Charles Adolphe Wurtz and others, Kekulé was the principal formulator of the theory of chemical structure ( 1857 – 58 ).
Kekulé is a lunar crater on the far side of the Moon.
By convention these features are identified on lunar maps by placing the letter on the side of the crater midpoint that is closest to Kekulé.

Kekulé and theory
Valence bond theory views aromatic properties of molecules as due to resonance between Kekulé, Dewar and possibly ionic structures, while molecular orbital theory views it as delocalization of the π-electrons.
Soon thereafter, Wurtz also adopted the new structural theory that was developing from the work of younger chemists such as August Kekulé.
In Ghent, Ladenburg worked for 6 months with Kekulé who introduced him to structural theory.

Kekulé and developed
This commonly seen model of aromatic rings, namely the idea that benzene was formed from a six-membered carbon ring with alternating single and double bonds ( cyclohexatriene ), was developed by Kekulé ( see History section below ).
The technique was developed by the organic chemist Friedrich August Kekulé von Stradonitz.

Kekulé and called
An ahnentafel list is sometimes called a " Kekulé " after Stephan Kekulé von Stradonitz.

Kekulé and which
He was open to the idea of divalent carbon, which Kekulé was not.
He provided many more resolved formulas in his paper than Kekulé had, and in two cases even suggested ( hetero ) cyclical formulas, which could have influenced Kekulé in his later suggestion of the benzene ring.
The hypnagogic state can provide insight into a problem, the best-known example being August Kekulé ’ s realization that the structure of benzene was a closed ring while half-asleep in front of a fire and seeing molecules forming into snakes, one of which grabbed its tail in its mouth.
The first, which was proposed by Kekulé in 1867, later proved to be closest to the true structure of benzene.

Kekulé and compounds
In organic chemistry, aromatic compounds contain atomic rings, such as benzene rings ( the Kekulé structure ) consisting of five or six, usually carbon, atoms.

Kekulé and were
Since ortho derivatives of benzene were never actually found in more than one isomeric form, Kekulé modified his proposal in 1872 and suggested that the benzene molecule oscillates between two equivalent structures, in such a way that the single and double bonds continually interchange positions .< ref >
Meyer's contributions also included the concept that the carbon atoms in benzene were arranged in a ring, although he did not propose the alternation of single and double bonds that later became included in the structure by August Kekulé.

. and S
During the period from 1 July 1960 through 31 January 1961, the Medical Museum was required to move to Temporary Building `` S '' on the Mall from Chase Hall.
I tested it in my scoped S & W and it was good enough to allow me to hit a chuck with every shot at 100 yards if I did my part by holding the handgun steadily.
, S & H,, and.
Add holes in top, forming `` S '' for salt and `` P '' for pepper.
According to Philippoff, the recoverable shear S is given by Af where **yc is the angle of extinction.
On C, from the point P at Af to the point Q at Af, we construct the chord, and upon the chord as a side erect a square in such a way that as S approaches zero the square is inside C.
As S increases we consider the two free corner points of the square, Af and Af, adjacent to P and Q respectively.
As S approaches T the square will be outside C and therefore both Af and Af must cross C an odd number of times as S varies from zero to T.
As S varies from zero to T, the values of S for which Af and Af cross C will be denoted by Af and Af respectively.
Now with P fixed at Af, Af-values occur when the corner Af crosses C, and are among the values of S such that Af.
The photocathode sensitivities S, phosphor efficiencies P, and anode potentials V of the individual stages shall be distinguished by means of subscripts 1, and 2, in the text, where required.
The luminous gain of a single stage with Af ( flux gain ) is, to a first approximation, given by the product of the photocathode sensitivity S ( amp / lumen ), the anode potential V ( volts ), and the phosphor conversion efficiency P ( lumen/watt ).
In practical situations there will be restrictions on the admissible operating conditions, and we regard the vectors as belonging to a fixed and bounded set S.
The set of vectors Af constitutes the operating policy or, more briefly, the policy, and a policy is admissible if all the Af belong to S.
Mr. Kililngsworth was a foreman with S and W Cafeteria.
Thus, if what is at issue is whether `` All S is P '', it is indifferent whether `` Some S is not P '' or `` No S is P '', since in either case the judgment in question is false.
Lincoln closely supervised the war effort, especially the selection of top generals, including commanding general Ulysses S. Grant.
Lincoln's assassination was the first assassination of a U. S. president and sent the nation into mourning.

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