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Episode 21
Episode 21

... Before World War II. A substitute for silk. 5. What was the first organic synthesis? Wöhler's synthesis of urea. 6. What is a hydrocarbon? A compound formed only of hydrogen and carbon atoms. 7. What is meant by an isomer? Two molecules that have the same formula but have different structures. 8. Ho ...
Episode 21
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... Before World War II. A substitute for silk. 5. What was the first organic synthesis? Wöhler's synthesis of urea. 6. What is a hydrocarbon? A compound formed only of hydrogen and carbon atoms. 7. What is meant by an isomer? Two molecules that have the same formula but have different structures. 8. Ho ...
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... In the last (most common) representation only the carbon chain is drawn. Each C is assumed to have 4 bonds to it, but the H are not explicitly written out. The longest continuous C chain determines the root name for the compound. If additional groups are bonded to the main chain, they are assigned a ...
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... sodium sulphate. Process: chromium trichloride reacts with aluminium and benzene with aluminium chloride  as catalyst. The buildet complex then reacts with sodium sulphate and forms Cr(C6H6)2.  Electron Counting in organometallic compounds: 18‐electon rule (N.V. Sigwick Rule): by applying this rule  ...
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Section 7.5~7.6 - www .alexandria .k12 .mn .us
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phenols - Gneet`s
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... In phenols the –OH group is attached to sp2 hybrid carbon of an aromatic ring and the oxygen atom of the hydroxyl group has two lone pairs of electrons and the bond angle in phenol is 109o. The C-O bond length in phenol (136pm) is slightly less than in methanol(412pm) due to resonance in aromatic ri ...
rev2
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... 7. Know about the structure of phenols. 8. Be able to name phenols 9. Phenols are more soluble in water than alcohols because they are more polar. Know about the chemical reactivity a. Phenols are acidic in water (carbolic acid) b. Be able to finish aromatic reactions with phenols. (They do not act ...
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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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