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  2. Infrared spectroscopy correlation table - Wikipedia

    en.wikipedia.org/wiki/Infrared_spectroscopy...

    An infrared spectroscopy correlation table (or table of infrared absorption frequencies) is a list of absorption peaks and frequencies, typically reported in wavenumber, for common types of molecular bonds and functional groups. [1] [2] In physical and analytical chemistry, infrared spectroscopy (IR spectroscopy) is a technique used to identify ...

  3. Dihydroxybenzenes - Wikipedia

    en.wikipedia.org/wiki/Dihydroxybenzenes

    Similar to other phenols, the hydroxyl groups on the aromatic ring of a benzenediol are weakly acidic. Each benzenediol can lose an H + from one of the hydroxyls to form a type of phenolate ion. The Dakin oxidation is an organic redox reaction in which an ortho - or para -hydroxylated phenyl aldehyde ( −CH=O ) or ketone ( >C=O ) reacts with ...

  4. IUPAC numerical multiplier - Wikipedia

    en.wikipedia.org/wiki/IUPAC_numerical_multiplier

    The numbers 200-900 would be confused easily with 22 to 29 if they were used in chemistry. khīlioi = 1000, diskhīlioi = 2000, triskhīlioi = 3000, etc. 13 to 19 are formed by starting with the Greek word for the number of ones, followed by και (the Greek word for 'and'), followed by δέκα (the Greek word for 'ten').

  5. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    The suffixes -diol, -triol, -tetrol, etc., are used for multiple −OH groups: Ethylene glycol CH 2 OHCH 2 OH is ethane-1,2-diol. If higher precedence functional groups are present (see order of precedence , below), the prefix "hydroxy" is used with the bonding position: CH 3 CHOHCOOH is 2-hydroxypropanoic acid.

  6. Benzene - Wikipedia

    en.wikipedia.org/wiki/Benzene

    Benzene is a natural constituent of petroleum and is one of the elementary petrochemicals. Due to the cyclic continuous pi bonds between the carbon atoms, benzene is classed as an aromatic hydrocarbon. Benzene is a colorless and highly flammable liquid with a sweet smell, and is partially responsible for the aroma of gasoline.

  7. Functional group - Wikipedia

    en.wikipedia.org/wiki/Functional_group

    Compounds that contain sulfur exhibit unique chemistry due to sulfur's ability to form more bonds than oxygen, its lighter analogue on the periodic table. Substitutive nomenclature (marked as prefix in table) is preferred over functional class nomenclature (marked as suffix in table) for sulfides, disulfides, sulfoxides and sulfones.

  8. List of chemistry mnemonics - Wikipedia

    en.wikipedia.org/wiki/List_of_chemistry_mnemonics

    An atom (or ion) whose oxidation number increases in a redox reaction is said to be oxidized (and is called a reducing agent). It is accomplished by loss of one or more electrons. The atom whose oxidation number decreases gains (receives) one or more electrons and is said to be reduced. This relation can be remembered by the following mnemonics.

  9. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    The formula Na 2 SO 3 denotes that the cation is sodium, or Na +, and that the anion is the sulfite ion (SO 2− 3). Therefore, this compound is named sodium sulfite. If the given formula is Ca(OH) 2, it can be seen that OH − is the hydroxide ion. Since the charge on the calcium ion is 2+, it makes sense there must be two OH − ions