Ketones from acid chlorides

Ketones can be synthesized from acid chlorides through a reaction called Friedel-Crafts acylation. This reaction involves the reaction of an acid chloride with a Lewis acid catalyst, such as aluminum chloride (AlCl3), to form an acylium ion intermediate. The acylium ion then undergoes a nucleophilic attack by an arene, which leads to the formation of…

Preparation of: Aldehydes

Aldehydes can be prepared by several methods. Some of the commonly used methods are: These are some of the methods used for the preparation of aldehydes. What is Required Preparation of: Aldehydes The required preparation of aldehydes depends on the method being used for their synthesis. However, some common laboratory equipment and reagents that may…

C-O bond cleavage reactions

C-O bond cleavage reactions involve breaking the bond between a carbon atom and an oxygen atom in a molecule. These reactions can occur through a variety of mechanisms, including homolytic cleavage, heterolytic cleavage, and acid-catalyzed cleavage. Homolytic cleavage occurs when the bond between carbon and oxygen is broken evenly, with each atom receiving one of…

Preparation by Williamson’s synthesis

Williamson’s synthesis is a method used to prepare ethers. The general reaction involves the reaction of an alkoxide ion with a primary alkyl halide or a primary alcohol with an alkyl halide in the presence of a strong base such as sodium or potassium hydroxide. The reaction mechanism involves the formation of an alkoxide ion…

Carboxylic Acids

Carboxylic acids are organic compounds that contain a carboxyl functional group (-COOH). This functional group consists of a carbonyl group (C=O) and a hydroxyl group (-OH) bonded to the same carbon atom. The general formula for carboxylic acids is R-COOH, where R represents a hydrocarbon chain or a hydrogen atom. Carboxylic acids can be classified…

Ketones

Ketones are organic compounds that contain a carbonyl group (C=O) bonded to two alkyl or aryl groups. They are produced by the liver from fatty acids during periods of low glucose availability, such as during fasting, prolonged exercise, or a low-carbohydrate diet. In the human body, ketones serve as an alternative source of energy when…

Conversion of alcohols into aldehydes

Alcohols can be converted into aldehydes through oxidation reactions. One commonly used method is the use of an oxidizing agent such as chromic acid (H2CrO4), pyridinium chlorochromate (PCC), or Jones reagent (a solution of chromic acid and sulfuric acid). The specific oxidizing agent and conditions used will depend on the alcohol being converted and the…

Thionyl chloride

Thionyl chloride (SOCl2) is a chemical compound that is commonly used as a reagent in organic chemistry for various reactions, such as the conversion of alcohols to alkyl chlorides, carboxylic acids to acid chlorides, and amides to nitriles. Thionyl chloride is a colorless to slightly yellowish liquid with a pungent odor. It is highly reactive…

ZnCl2/Concentrated HCl

ZnCl2 is the chemical formula for zinc chloride, and HCl is the chemical formula for hydrochloric acid. When these two substances are combined, they react to form a complex mixture of products. The reaction between ZnCl2 and HCl is exothermic, meaning that it releases heat as it proceeds. The products of the reaction include hydrogen…

Phosphorus halides

Phosphorus halides are compounds formed by the combination of phosphorus with halogens (fluorine, chlorine, bromine, iodine). The most common phosphorus halides are phosphorus trichloride (PCl3), phosphorus pentachloride (PCl5), phosphorus tribromide (PBr3), and phosphorus triiodide (PI3). Phosphorus trichloride (PCl3) is a colorless liquid with a pungent odor. It is used in the production of pesticides, herbicides,…