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15. Thermosets from Renewable Sources
15. Thermosets from Renewable Sources

... that has been converted to benzene. Those methods directly discriminate between product carbon resulting from new carbon input and that derived from fossil-based input. A measurement of the 14C/12C ratio is determined relative to the modern carbonbased oxalic acid radiocarbon Standard Reference Mate ...
102 Lecture Ch15
102 Lecture Ch15

... have higher boiling points than hydrocarbons • However, they have no H attached to the O, so do not have hydrogen bonding, and have lower boiling points than alcohols • Like ethers, aldehydes and ketones can hydrogen bond with water, so those with less than 5 carbons are generally soluble in water • ...
Chapter 1 Structure and Bonding
Chapter 1 Structure and Bonding

... Modified LiAlH4 reagent LiAl[OC(CH3)3]3H required to prevent over-reduction to alcohols ...
Unit-5-Lipids
Unit-5-Lipids

... carbohydrates, and lipids. The lipids are the subject of this unit. Of these four families, the lipids are the structurally the most diverse. This is because unlike members of the other three families, members of this families do no share a common structural feature, but rather share a common physic ...
Chemistry 2100 - Bonham Chemistry
Chemistry 2100 - Bonham Chemistry

... – Both IUPAC and common names of esters are derived from the names of the parent carboxylic acids. – Name the alkyl or aryl group bonded to oxygen first, followed by the name of the acid; replace the suffix -ic acid by -ate. – A cyclic ester is called a lactone. ...
asymmetric alkyne addition to aldehydes
asymmetric alkyne addition to aldehydes

... Chiral propargylic alcohols are important compounds, as this structural motif is often found in pharmaceutical compounds as well as natural products and can also serve as versatile synthetic intermediates.1 Although there are many methods available for the preparation of these compounds (e.g. asymme ...
Unit-5-LipidsClick copy
Unit-5-LipidsClick copy

... carbohydrates, and lipids. The lipids are the subject of this unit. Of these four families, the lipids are the structurally the most diverse. This is because unlike members of the other three families, members of this families do no share a common structural feature, but rather share a common physic ...
Organic Chemistry Organic Chemistry
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... With the huge number of organic substances, we would have great difficulty memorizing the properties of each compound. Fortunately, the compounds fall into organic families according to particular combinations of atoms in each molecule. The physical properties and reactivity of the compounds are rel ...
Şenol, O.İ., Viljava, T.-R., Krause, AOI
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... Methyl heptanoate and methyl hexanoate did not react at 300 8C without catalysts. The alumina support converted about 13% of the esters at 300 8C and the identified products included only the alcohols and the acids. Although the alumina support had some activity for deesterification and dehydration ...
Chemistry Notes for class 12 Chapter 12 Aldehydes, Ketones and
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... potassium tartrate which is also called, Rochelle salt.] (c) Benedict solution With it, aldehydes (except benzaldehyde) also give red ppt. of CU2O. (d) Schiff’s reagent It is an aqueous solution of magenta or pink coloured rosaniline hydrochloride which has been decolourised by passing SO2, Aldehyde ...
Synthesis of Novel Steroid-Peptoid Hybrid Macrocycles by
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... replaced by an azido group with retention of configuration, followed by ester hydrolysis and azide reduction. Upon reaction of this amino acid building block with an oxo component and an isocyanide under dilution conditions, a mixture of the cyclodimer 18 and the cyclotrimer 19 were obtained in 33% ...
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... • Fatty acids which can’t be synthesized by the body are essential fatty acids – Linoleic acid is an essential fatty acid required to make arachadonic acid ...
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... • Chlorine and iodine can be introduced into aromatic rings by electrophilic substitution reactions, but fluorine is too reactive, and only poor yields of monofluoroaromatic products are obtained by direct fluorination. For example: H ...
Fatty Acids - dan
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... • Fatty acids which can’t be synthesized by the body are essential fatty acids – Linoleic acid is an essential fatty acid required to make arachadonic acid ...
View/Open
View/Open

... Development of Chemical Bonding Theory 7 The Nature of Chemical Bonds: Valence Bond Theory 10 sp3 Hybrid Orbitals and the Structure of Methane 12 sp3 Hybrid Orbitals and the Structure of Ethane 14 sp2 Hybrid Orbitals and the Structure of Ethylene 15 sp Hybrid Orbitals and the Structure of Acetylene ...
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... General characteristics of these chemicals: -Acyclic (e.g., no benzene rings) -Cyclic but does not contain a likely H-bonding group; ...
Topic 10.4 Organic Chemistry Alcohols
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... The physical properties of alcohols are similar to those of both water and hydrocarbons The shorter chain alcohols such as methanol and ethanol are similar to water, in general they -- have higher boiling points than hydrocarbons but lower than water -- dissolve in water to some degree -- are more p ...
Pharmacognosy-I (Part-7)
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... atoms (usually in a heterocyclic ring) and they usually have a marked physiological action on man or other animals. • The name 'proto-alkaloid' or 'amino-alkaloid' is sometimes applied to compounds such as hordenine, ephedrine and colchicine which lack one or more of the properties of typical alkalo ...
Aldehydes and ketones
Aldehydes and ketones

... In these compounds, the carbonyl group is bound to a nitrogen (an amino group), in addition to either a H-atom or a carbon group (alkyl, cycloalkyl, aromatic). The R’ and R” groups of the amino group may either be H or carbon groups: General formula for an amide: ...
Aldehydes and ketones
Aldehydes and ketones

... • Neither aldehydes nor ketones possess the ability to H-bond with other molecules like themselves. Consequently, boiling points for aldehydes and ketones are lower than for alcohols of similar molar mass. • The C-O double bond in these molecules is polar, so dipoledipole forces do exist. As a resul ...
ug chemistry - Krishna University
ug chemistry - Krishna University

... Nucleophilic aliphatic substitution reaction- classification into SN1 and SN2. Energy profile diagram of SN1 and SN2 reactions. Stereochemistry of SN2 (Walden Inversion) SN1 (Racemisation). Explanation of both by taking the example of optically active alkyl ...
Chapter 21 Carboxylic Acid Derivatives
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... • Soaps are made by heating NaOH with a fat (triester of glycerol) to produce the sodium salt of a fatty acid - a soap. • One example of a soap is sodium stearate, Na+ -OOC(CH2)16CH3. ...
Document
Document

... OH group-containing compounds (8) are by far the most important reactants for isocyanates. They are added under mild conditions, forming carbamic esters (9). Primary alcohols, secondary alcohols, and phenols show decreasing reactivity in that order. ...
13.1 Alcohols and Phenols 13.1 Alcohols and Phenols 13.1
13.1 Alcohols and Phenols 13.1 Alcohols and Phenols 13.1

... Methanol (CH3OH) is the most simple alcohol. With a suitable catalyst, about 2 billion gallons of  methanol are made industrially from CO2 and H2 every  year. Methanol is quite poisonous, but it has many uses as: 1. Solvent  2. Precursor for chemical syntheses  ...
Reactions of Acyl Chlorides
Reactions of Acyl Chlorides

... normally, symmetrical anhydrides are used (both R groups the same) reaction can be carried out in presence of pyridine (a base) or it can be catalyzed by acids ...
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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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