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g - Porterville College Home
g - Porterville College Home

... prefixes. Do not allow other instances of Greek or similar prefixes to confuse use in naming some of the oxyanions. For example, Cr2O72- is named dichromate. This has nothing to do with the naming of binary molecular compounds. There are a few instances of oxyanions series for a non-metal with two ...
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CBA 2

... 9. Elements are arranged in a certain order in the periodic table, from left to right and top to bottom. A pattern of repeating physical and chemical properties of the elements emerges. What is this order of arrangement? A. alphabetical order of the masses of the elements B. increasing order of the ...
Compounds of Carbon
Compounds of Carbon

... Compounds of Carbon Carbon is an important element as it forms 90% of all chemical compounds and forms the basis of living systems. The chemistry involving carbon was known as organic chemistry, as this term indicated carbons’ importance in living organisms. Carbon is most commonly found in compound ...
Synthesis of Benzene Derivatives: Electrophilic Aromatic Substitution
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... then continues in a direction (clockwise or counter-clockwise) that affords the second substituent the lower possible location number. 4. If several substituents are present on the ring, they are listed in alphabetical order. Location numbers are assigned to the substituents so that one of them is a ...
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The Chemistry of Life: Organic Compounds

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Photosynthesis Stores Energy in Organic Compounds

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Photosynthesis Stores Energy in Organic Compounds

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Review for Physical Science Test #2

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What Are Compounds? - Parma School District

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polar covalent bonds.
polar covalent bonds.

... •Each element can be assigned an electronegativity value which represents its electron accepting ability when participating in a chemical bond. •The larger the difference in electronegativety between two atoms participating in a chemical bond, the more ionic is the bond. •Bonds between atoms of diff ...
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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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