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Profile Documents Logout
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Chemistry English
Chemistry English

... much too small to be weighted. It is possible to compare the weights of a large number of atoms of element A with that of the same number of atoms of element B. Atomic Weights for elements are determined by comparing a very large number of the atoms of the element with the same number of atoms of C- ...
CHEM 263 (AS 40) Organic Chemistry II Winter 2017 Instructor: Dr
CHEM 263 (AS 40) Organic Chemistry II Winter 2017 Instructor: Dr

... • Apply chemical concepts learned in the lecture to laboratory situations and vice versa. • Identify and name a variety of organic functional groups (alkenes, alkynes, alcohols, phenols, ethers, aromatic compounds, aldehydes, ketones, amines, carboxylic acids and carboxylic acid derivatives). Draw s ...
Electronic Supplementary Information (ESI) service
Electronic Supplementary Information (ESI) service

... Complex 8 was prepared by addition of a toluene solution (1 eq) of 5 (5 mol%) into a toluene solution of the complex PhPH2-BH3 cooled at -20°C. Evolution of hydrogen was immediately observed. The reaction was completed after one night to 0°C. Product is thermally unstable and should be kept in solut ...
Unit 3 - High School Chemistry
Unit 3 - High School Chemistry

Chapter 2 Notes
Chapter 2 Notes

... Carbon atoms can form diverse molecules by bonding to four other atoms • Electron configuration is the key to an atom’s characteristics • Electron configuration determines the kinds and number of bonds an atom will form with other atoms Copyright © 2008 Pearson Education, Inc., publishing as Pearso ...
5.2. Related mechanisms of halogen chemistry A large variety of
5.2. Related mechanisms of halogen chemistry A large variety of

... can also occur at other unsaturated bonds of the reactive SOA or at aromatic systems. αpinene induced SOA is suspected to be rather poor on unsaturated bonds. SOA from catechol and guaiacol still exhibits a large amount of unsaturated or aromatic structural elements. Furthermore, these reactions tak ...
T. V. RajanBabu Chemistry, 730 Autumn 1997
T. V. RajanBabu Chemistry, 730 Autumn 1997

... Axial vs equatorial approach to cyclic carbonyl compounds by nucleophiles Klein / Cieplak models Tortional interactions in bicyclic systems Ring closure and ring size (Baldwin’s rules) - enthalpy and entropy of activation Bürgi-Dunitz angle, Radical cyclization reactions under kinetic vs thermodynam ...
730-2005 topics
730-2005 topics

... Axial vs equatorial approach to cyclic carbonyl compounds by nucleophiles Klein / Cieplak models Tortional interactions in bicyclic systems Ring closure and ring size (Baldwin’s rules) - enthalpy and entropy of activation Bürgi-Dunitz angle, Radical cyclization reactions under kinetic vs thermodynam ...
Lecture 16 Aromatic Diazonium Salts
Lecture 16 Aromatic Diazonium Salts

... Aromatic azo-compounds are coloured. Several of those compounds synthesized by the diazo-coupling are employed as dye-stuffs. These compounds can be classified into three groups. ...
Fig. 7
Fig. 7

... Substituent alkyl groups at positions 2 & 4 not 4 & 6. ...
Chemical properties of amines:
Chemical properties of amines:

... values slightly higher than amonia. Thus aliphatic amines are stronger bases than amonia. Like amonia, compounds with amino groups can also neutralize hydronium ions. This neutralization occurs very rapidly and essentially goes to completion at room temperature. Protonated amine cations can neutrali ...
SCH 4C - mscucinato
SCH 4C - mscucinato

... 1. Study the WHMIS symbols on page 479. 2. What does the term qualitative analysis refer to? Give an example of a time where you carried out a qualitative analysis in class. 3. Distinguish between physical properties and chemical properties. Give an example of each. 4. Distinguish between physical c ...
Stereochemistry and Stereoisomers Revisited
Stereochemistry and Stereoisomers Revisited

... The monochromatic light source of a polarimeter is generally a sodium lamp. The light waves are directed through a polarizer, and the emerging plane-polarized light passes through the sample. Finally, the light passes through an analyzer. If the plane of the light is not altered by the sample, the c ...
The Chemistry of Essential Oils - chemistryteaching / Chemistry
The Chemistry of Essential Oils - chemistryteaching / Chemistry

... – each of which should be evident from the diagram or in the explanation (1). Laboratory synthesized carvone would be a racemic mixture because there would be equal quantities of the (+) and (– )isomers or enantiomers (1). However, when an optically active compound is synthesised naturally – for exa ...
Topic 16 Test - A
Topic 16 Test - A

... How many structural isomers, which are aldehydes, have the molecular formula C5H10O? A ...
CLASS X carbon and its compound
CLASS X carbon and its compound

... atoms are attached to the main straight chain of carbon atoms by a single covalent bond are called branched chain hydrocarbons. 13. Isomerism : The phenomenon due to which there can exist two or more organic compounds, with different physical and chemical properties, due to the difference in arrange ...
CP - Fundamentals
CP - Fundamentals

Chemistry 11
Chemistry 11

... Chemists use oxidation numbers to keep track of the positive or negative character of atoms or ions. When electrons are removed completely or shifted partially away from an atom during a chemical reaction, the atom is given a more positive oxidation number. When electrons are gained or shifted towar ...
Chapter 3
Chapter 3

... • The parent name is that of the longest chain that contains the C=C. • Number the chain from the end that gives the lower numbers to the carbons of the C=C. • Locate the C=C by the number of its first carbon. • Use the ending -ene to show the presence of the C=C • Branched-chain alkenes are named i ...
Chapter 1 Review, pages 72–77
Chapter 1 Review, pages 72–77

... (a) From the name 2-chloro-2-butyne, carbon number 2 in the 4-carbon chain forms a carbon single bond with carbon number 1 and a triple bond with carbon number 3, and with a chlorine atom bonded to it. Altogether, this carbon number 2 forms five bonds. Since a carbon can form at most four bonds, the ...
Functional Groups
Functional Groups

... Functional Groups A specific arrangement of atoms in an organic compound that is capable of characteristic chemical reactions. In other words, a substituent group other than an alkyl group. Most organic chemistry is functionalgroup chemistry. We will do one functional group. ...
1H NMR - INTEC Chemistry Blog
1H NMR - INTEC Chemistry Blog

... 3. Area under the peak = relative number of H in that chemical environment ...
Alkanes
Alkanes

... However, carbons in butane (C4H10) can be arranged in two ways; four carbons in a row (linear alkane) or a branching (branched alkane). These two structures are two constitutional isomers for butane. Number of possible structures increases with the number of carbons in the molecule. Prentice Hall © ...
315.pdf
315.pdf

... to dominate. As the temperature is lowered, the RKKY interaction overtakes the Kondo interaction. Hence, the system orders ferromagnetically at low temperatures. The magnetic-ordering temperature T~ of CePdSb is higher than the T~ of GdPdSb as well as the T~ =13 K of orthorhombic EuPdSb (in which Eu ...
Main-group elements as transition metals
Main-group elements as transition metals

... distortion (that is, bending) increases as the group is descended, and it is possible to write these distorted structures using a valencebond approach (Fig. 1d), analogous to Lappert’s representations of the ethylene analogues (Fig. 1b and c). In essence, the heavier alkyne analogues also contain an ...
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Homoaromaticity



Homoaromaticity in organic chemistry refers to a special case of aromaticity in which conjugation is interrupted by a single sp3 hybridized carbon atom. Although this sp3 center disrupts the continuous overlap of p-orbitals, traditionally thought to be a requirement for aromaticity, considerable thermodynamic stability and many of the spectroscopic, magnetic, and chemical properties associated with aromatic compounds are still observed for such compounds. This formal discontinuity is apparently bridged by p-orbital overlap, maintaining a contiguous cycle of π electrons that is responsible for this preserved chemical stability.The concept of homoaromaticity was pioneered by Saul Winstein in 1959, prompted by his studies of the “tris-homocyclopropenyl” cation. Since the publication of Winstein's paper, much research has been devoted to understanding and classifying these molecules, which represent an additional “class” of aromatic molecules included under the continuously broadening definition of aromaticity. To date, homoaromatic compounds are known to exist as cationic and anionic species, and some studies support the existence of neutral homoaromatic molecules, though these are less common. The 'homotropylium' cation (C8H9+) is perhaps the best studied example of a homoaromatic compound.
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