Chemistry of Organic Compounds
Organic chemistry. Chemical bonds and intermolecular forces. Chemical reactivity. Isolation and analysis of organic compounds. Alkanes. Alkanes cyclic hydrocarbons. Natural gas and petroleum. Alkyl halides. organic acids. Infrared spectra. Ethers. Synthesis of alkanes and alkanes (acetylenes). Carboxylic acids and their derivatives. ortho esters. peroxy acids and their derivatives. Waxes, fats, and oils. aldehydes and ketones. Aliphatic nitrogen compounds. Aliphatic compounds of some third and higher period elements. Derivatives of carbonic acid and of tiocarbonic acid. Optical isomerism. Carbohydrates. Amino acids, proteins, and peptides. Aromatic hydrocarbons and peptides. Aromatic hydrocarbons. sources of aromathic compounds infrared spectra. Halogen derivatives of aromatic hydrocarbons. Aromatic sulfonic acids and their derivatives. Aromatic nitro compounds. Aromatic smines and phosphines. Aromatic diazo compounds. Phenols, aminophenols, and quinones. Aromathic alcohols, aralkylamines, aldehydes, and ketones stereochmistry of the Oximes. Aromatic carboxylic acides and their derivatives. Arylalkanes, free radicals. Arylalkenes and arylalkynes biphenyl and its derivatives. Condensed nuclear aromatic compounds. Heterocyclic compounds nucleic acids alkaloids. Mass spectrometry, nuclear magnetic and electron paramagnetic resonance, electronic absorption spectra. Color. dyes and dyeing. organic pigments. Polyenes. Rubber and synthetic rubbers. Chlorinated and fluorinated aliphatic hydrocarbons. Unsaturated alcohols, Epoxides, polyhydric alcohols, amino alcohols, and polyamines. Hydroxy, Unsaturated, halogenated, and amino carbonyl compounds dicarbonyl compounds. Halogenated, hydroxy, amino, and unsaturated acides. Polycarboxylic acids. Keto acids. Nonbenzenoid cyclic compounds. Terpenes and steroids biogenesis.
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Chemical Bonds and Intermolecular Forces
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absorption acetic acid acetylene acyl addition alcohol aldehydes alkali alkanes alkyl groups alkyl halides amide amines amino acids amino group ammonia ammonium anhydride aniline aromatic benzene boiling bromide carbon atom carbonyl group carboxylic acids catalyst cent CH2OH chemical CHOH color converted cyanide derivatives dioxide distillation double bond dyes energy esters ether ethylene fluoride formaldehyde formation formula free radical give glycol Grignard reagents halogen heated Hence hybrid hydrocarbons hydrogen atoms hydrogen chloride hydrolysis hydrolyzed hydroxyl group intermediate iodide isolated isomeric isomers kcal ketones known liquid methyl mixture mole molecular weight molecule NaOH nitro nitrogen nucleophilic obtained olefins orbitals ortho oxidation oxygen pair of electrons peroxide phenol polymerization position pounds prepared presence proteins proton pyridine react reaction reactive readily reduction resonance ring salt sodium hydroxide soluble solvent stable structure substitution sulfate sulfide sulfonic sulfuric acid synthesis takes place temperature tertiary tion unsaturated yields