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Organic Reactions
Organic Reactions

... Esters are an important class of organic compounds commonly prepared from the esterication reaction of an organic acid with an alcohol in the presence of a strong mineral acid (usually H2 SO4 ). They are chiey responsible for the pleasant aromas associated with various fruits, and as such are used ...
Topics 10 and 20 Outline
Topics 10 and 20 Outline

... Use of data—much of the progress that has been made to date in the developments and applications of scientific research can be mapped back to key organic chemical reactions involving functional group interconversions. (3.1) Understandings: • Alkanes have low reactivity and undergo free-radical subst ...
Benzoic Acid
Benzoic Acid

... biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Ascorbic acid is easily oxidized and is used as a reductant in photographic developer solutions (among others) and as a preservative. A vitamin used in preventing scurvy, as a strong reduci ...
The presence of an aromatic ring or other
The presence of an aromatic ring or other

... part of organic chemistry. Although it is often possible to establish the structure of a compound on the basis of spectra alone (IR, NMR, etc.), the spectra typically must be supplemented with other information about the compound: physical state and properties (melting point, boiling point, solubili ...
Carboxylic Acid Structure and Chemistry
Carboxylic Acid Structure and Chemistry

... conditions" nucleophiles can attack the acids carbonyl and displace the acid OH as water, or another good leaving group. Such is the case in esterification reactions performed under acidic conditions. In these reactions an acid is treated with an alcohol which serves as the nucleophile, and an acid ...
Chemistry 11 Fall 2009 Examination #5
Chemistry 11 Fall 2009 Examination #5

... Lipids are soluble in liquid ammonia. Lipids are classified based on their property of solubility rather than their structure. Lipids are soluble in CCl4. Lipids form an integral part of the cell membrane. Lipids store energy within fat cells. ...
carbohydrates
carbohydrates

... Two glucose molecules react with each other; one of them (showing on the left side) participates in the reaction with its glycosidic –OH group, forming a glycosidic ether or glycoside. The other glucose (right side) participates with an ordinary secondary alcoholic hydroxyl group. The product is cal ...
WHAT IS MORPHINE -- ACTIVITY #1 What is morphine? What is it
WHAT IS MORPHINE -- ACTIVITY #1 What is morphine? What is it

... Primary alcohols can be oxidised to aldehydes and on to carboxylic acids. (It can be difficult to stop the oxidation at the aldehyde stage.) Secondary alcohol - Secondary alcohols have an -OH function attached to a R2CH- group. Secondary alcohols can be oxidised to ketones. Tertiary alcohol - Tertia ...
Chapter 12 Alcohols from Carbonyl Compounds: Oxidation
Chapter 12 Alcohols from Carbonyl Compounds: Oxidation

... Solved Problem: Synthesize the following compound using an alcohol of not more than 4 carbons as the only organic starting material ...
Chapter 1-
Chapter 1-

... Solved Problem: Synthesize the following compound using an alcohol of not more than 4 carbons as the only organic starting material ...
Nuggets of Knowledge - Dixie State University
Nuggets of Knowledge - Dixie State University

... Line structure: carbon atoms are not shown, only the bonds between them; hydrogen atoms and their bonds are not shown, unless they are attached to an atom other than carbon; nonbonding electron pairs are always shown. ...
carboxylic acid
carboxylic acid

... CHOH CH2OH ...
The Amino Acids
The Amino Acids

... Only four electrons in the outer shell ...
File - Dr KHALID SHADID
File - Dr KHALID SHADID

... Reactions of Carboxylic Acid Anhydrides Because carboxylic acid anhydrides are highly reactive they can be used to prepare esters and amides. ...
10. Chemistry in Everyday Life
10. Chemistry in Everyday Life

... using it. b. Antioxidants in food: The chemical substance that retards the action of oxygen on food during preservation is called antioxidant. These are more reactive towards oxygen than the food material which they are protecting. E.g.: Butylated hydroxy toluene (BHT) and butylated hydroxy anisole ...
Nomenclature of Organic Compounds
Nomenclature of Organic Compounds

... EX. 2,3-dimethylhexane Cycloalkanes: 1. Ring is parent unless the substituent has more Cs than the ring 2. If the ring has a. Only one substituent do NOT number it b. Two substituents, cite them alphabetically and give the number 1 position to the first substituent. c. Three or more substituents, th ...
OCR A Level Chemistry B (Salters) Multiple Choice Questions Quiz
OCR A Level Chemistry B (Salters) Multiple Choice Questions Quiz

... We’d like to know your view on the resources we produce. By clicking on ‘Like’ or ‘Dislike’ you can help us to ensure that our resources work for you. When the email template pops up please add additional comments if you wish and then just click ‘Send’. Thank you. If you do not currently offer this ...
ch14[1].
ch14[1].

... • By careful control of experimental conditions, it is possible to prepare esters in high yield. • If the alcohol is inexpensive relative to the carboxylic acid, it can be used in excess to drive the equilibrium to the ...
DMF
DMF

... mechanisms, such as SN2 reactions. Dimethylformamide can be synthesized from methyl formate anddimethylamine or by reaction of dimethylamine with carbon monoxide. Dimethylformamide is reactive toward strong bases such as sodium hydroxide or strong acids such as hydrochloric acid or sulfuric acid and ...
Lectures 37-38 - U of L Class Index
Lectures 37-38 - U of L Class Index

... solution, but the pKa scale doesn’t just go from 0 to 14! Often times, the solvent for a reaction is chosen based (at least in part) ...
Lectures 37-38 - U of L Class Index
Lectures 37-38 - U of L Class Index

... solution, but the pKa scale doesn’t just go from 0 to 14! Often times, the solvent for a reaction is chosen based (at least in part) ...
CHEM 212B, Organic Chemistry - City College of San Francisco
CHEM 212B, Organic Chemistry - City College of San Francisco

... 3. Lab text: Techniques in Organic Chemistry, Mohrig, Hammond, Schatz, 3rd ed., 2010, (W.R. Freeman and Co.) 4. Computer-assisted organic chemistry learning aids in the CCSF Chemistry department ...
1 per page - TeachLine
1 per page - TeachLine

... •  Ketone bodies are released by liver to bloodstream •  Organs other than liver can use ketone bodies as fuels •  Too high levels of acetoacetate and βhydroxybutyrate lower blood pH dangerously ...
File - need help with revision notes?
File - need help with revision notes?

... Phenyl Ethanoate + Ethanoic acid Conditions: Ethanoic Anhydride / methanol /warm ...
organic functional group analysis
organic functional group analysis

... This experiment will introduce you to some of the more common functional groups of organic chemistry. The functional group is that portion of the molecule that undergoes a structural change during a chemical reaction. The functional groups that will be studied in this experiment are carboxylic acid, ...
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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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