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Organic Chemistry - UCR Chemistry
Organic Chemistry - UCR Chemistry

... deprotonation. The three "chromate" species, or the three "dichromate" species, are simply differently protonated froms of CrO4-2 or Cr2O7-2, respectively Unwanted Oxidation of Aldehydes. Cr(VI) reagents are powerful oxidizing agents useful for oxidizing 2° alcohols to ketones (Figure 17.005) becaus ...
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SQA CfE Higher Chemistry Unit 2
SQA CfE Higher Chemistry Unit 2

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O-VOCS - Tubitak Journals
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Chemistry 30 - SharpSchool
Chemistry 30 - SharpSchool

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carboxylic acids and their derivatives
carboxylic acids and their derivatives

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Chapter 22 Summary - McGraw Hill Higher Education
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A Crash Course In Organic Chemistry
A Crash Course In Organic Chemistry

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Enzymatic synthesis of bioactive compounds

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Protection (and Deprotection) of Functional Groups in Organic
Protection (and Deprotection) of Functional Groups in Organic

... (CA), such as many clays, zeolites, and metal oxides. In some instances, due to their insufficient acidity, prolonged reaction times or a large quantity of them are usually necessary, and, consequently, they are often modified by treatment with Lewis acids or protic acids (SA) to increase their cata ...
Chemistry - Andhra University
Chemistry - Andhra University

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CHM102 - National Open University of Nigeria
CHM102 - National Open University of Nigeria

... identify the functional groups present in a molecule give IUPAC names of various compounds belonging to different classes • write the correct structure of a compound from its name. ...
Amines
Amines

... pair on N lies in an sp2 hybrid orbital (33% s character) and is held more tightly to the nucleus than the free electron pair on N in an sp3 hybrid orbital (25% s character) ...
organic families
organic families

... a Place 5 drops of the liquid in a test tube and add 2 drops of universal indicator solution. b Carefully smell the liquid. c Place 1 mL of the liquid in a test tube. Add 1 mL of sulfuric acid solution and 10 drops of potassium dichromate solution. Stand the test tube in a hot water bath for two min ...
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Phenols



In organic chemistry, phenols, sometimes called phenolics, are a class of chemical compounds consisting of a hydroxyl group (—OH) bonded directly to an aromatic hydrocarbon group. The simplest of the class is phenol, which is also called carbolic acid C6H5OH. Phenolic compounds are classified as simple phenols or polyphenols based on the number of phenol units in the molecule.Synonyms are arenols or aryl alcohols.Phenolic compounds are synthesized industrially; they also are produced by plants and microorganisms, with variation between and within species.Although similar to alcohols, phenols have unique properties and are not classified as alcohols (since the hydroxyl group is not bonded to a saturated carbon atom). They have higher acidities due to the aromatic ring's tight coupling with the oxygen and a relatively loose bond between the oxygen and hydrogen. The acidity of the hydroxyl group in phenols is commonly intermediate between that of aliphatic alcohols and carboxylic acids (their pKa is usually between 10 and 12).Loss of a positive hydrogen ion (H+) from the hydroxyl group of a phenol forms a corresponding negative phenolate ion or phenoxide ion, and the corresponding salts are called phenolates or phenoxides, although the term aryloxides is preferred according to the IUPAC Gold Book. Phenols can have two or more hydroxy groups bonded to the aromatic ring(s) in the same molecule. The simplest examples are the three benzenediols, each having two hydroxy groups on a benzene ring.Organisms that synthesize phenolic compounds do so in response to ecological pressures such as pathogen and insect attack, UV radiation and wounding. As they are present in food consumed in human diets and in plants used in traditional medicine of several cultures, their role in human health and disease is a subject of research.ref name=Klepacka Some phenols are germicidal and are used in formulating disinfectants. Others possess estrogenic or endocrine disrupting activity.
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