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Le Chatelier’s principle

Le Chatelier’s principle

Le Chatelier’s principle – In 1884, the French Chemist Henry Le Chatelier proposed a general principle which applies to all systems in equilibrium. This important principle called the Le Chatelier’s principle may be stated as : when a stress is applied on a system in equilibrium, the system tends to …

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Oxidation of Alcohols

Oxidation of Alcohols

Oxidation of Alcohols – Primary and secondary alcohols are easily oxidized (Oxidation of Alcohols)  by a variety of reagents, including chromium oxides, permanganate, nitric acid, and even household bleach (NaOCl, sodium hypochlorite). – The choice of reagent depends on the amount and value of the alcohol. – We use cheap …

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Thiols (Mercaptans)

What is Thiols? – Thiols are sulfur analogues of alcohols, with an -SH group in place of the alcohol -OH group. – Oxygen and sulfur are in the same column of the periodic table (group 6A), with oxygen in the second row and sulfur in the third. Nomenclature of Thiols …

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Law of Mass action

Law of Mass action

Law of Mass action – Two Norwegian chemists, Guldberg and Waage, studied experimentally a large number of equilibrium reactions. In 1864, they postulated a generalisation called the Law of Mass action. – Law of Mass action states that : the rate of a chemical reaction is proportional to the active …

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Side Reactions of Organometallic Reagents

Side Reactions of Organometallic Reagents

Side Reactions of Organometallic Reagents: Reduction of Alkyl Halides – Organometallic Reagents: Grignard and organolithium reagents are strong nucleophiles and strong bases. – Besides their additions to carbonyl compounds, they react with other acidic or electrophilic compounds. – In some cases, these are useful reactions, but they are often seen …

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Organometallic Reagents for Alcohol Synthesis

Organometallic Reagents for Alcohol Synthesis

Organometallic Reagents for Alcohol Synthesis – Organometallic compounds contain covalent bonds between carbon atoms and metal atoms. –  And Organometallic reagents are useful because they have nucleophilic carbon atoms, in contrast to the electrophilic carbon atoms of alkyl halides. – Most metals (M) are more electropositive than carbon, and the …

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Acidity of Alcohols and Phenols

Acidity of Alcohols and Phenols

Acidity of Alcohols and Phenols – we will talk here about some Acidity of Alcohols and Phenols. – Like the hydroxyl proton of water, the hydroxyl proton of an alcohol is weakly acidic. – A strong base can remove the hydroxyl proton to give an alkoxide ion. – The acidities …

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Commercially Important Alcohols

Commercially Important Alcohols

we will talk about some Commercially Important Alcohols such as:  Methanol , Ethanol , isopropyl alcohol (1) Commercially Important Alcohols: Methanol  – Methanol (methyl alcohol) was originally produced by the destructive distillation of wood chips in the absence of air. This source led to the name wood alcohol. – During …

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Physical Properties of Alcohols

Physical Properties of Alcohols

We will discuss here Physical Properties of Alcohols: (A) Boiling Points of Alcohols (B) Solubility Properties of Alcohols Physical Properties of Alcohols – Most of the common alcohols, up to about 11 or 12 carbon atoms, are liquids at room temperature. – Methanol and ethanol are free-flowing volatile liquids with …

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Nomenclature of Alcohols and Phenols

Nomenclature of Alcohols and Phenols

In this subject we will talk about Nomenclature of Alcohols and Phenols (1) Nomenclature of Alcohols: IUPAC Names – The IUPAC system provides unique names for alcohols, based on rules that are similar to those for other classes of compounds. – In general, the name carries the (-ol) suffix, together …

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Reactions of Alkynes

Reactions of Alkynes

Reactions of Alkynes – Many of the reactions of alkynes are similar to the corresponding reactions of alkenes because both involve pi bonds between two carbon atoms. – Like the pi bond of an alkene, the pi bonds of an alkyne are electron-rich, and they readily undergo addition reactions. (A) …

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