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Showing posts from December, 2017

PERIODICITY

NON-IDEAL MIXTURES OF LIQUIDS

What is non-ideal solution example? What is an ideal mixture of liquids? How does liquid mixture deviate from ideal behavior? What is ideal and non-ideal? What is difference between ideal and non-ideal solution? NON-IDEAL MIXTURES OF LIQUIDS DOWNLOAD THE NOTES 

POLYAMIDES

What are examples of polyamides? What is polyamide in chemistry? Is polyamide a plastic? Why are proteins called polyamides? Why are polyamides so strong? What kind of fabric is polyamide? POLYAMIDES DOWNLOAD THE NOTES 

REACTIONS BETWEEN HALOGENOALKANES AND AMMONIA

What reacts with halogenoalkanes? What happens when alkyl halide reacts with ammonia? What happens when ethanol react with ammonia? What happens when ethyl bromide reacts with ammonia? Why do Halogenoalkanes undergo substitution reactions? Are Halogenoalkanes reactive? REACTIONS BETWEEN HALOGENOALKANES AND AMMONIA DOWNLOAD THE NOTES 

REDUCTION OF CARBOXYLIC ACIDS

Does carboxylic acid undergo reduction?, Does NaBH4 reduce carboxylic acids?, Which reagent is preferred for the reduction of carboxylic acids?, Why are carboxylic acids hard to reduce?, What reactions do carboxylic acids undergo? REDUCTION OF CARBOXYLIC ACIDS DOWNLOAD THE NOTES 

HYDROLYSING NITRILES

HYDROLYSING NITRILES This page looks at the hydrolysis of nitriles under either acidic or alkaline conditions to make carboxylic acids or their salts. The hydrolysis of nitriles Introduction When nitriles are hydrolysed you can think of them reacting with water in two stages - first to produce an amide, and then the ammonium salt of a carboxylic acid. For example, ethanenitrile would end up as ammonium ethanoate going via ethanamide. In practice, the reaction between nitriles and water would be so slow as to be completely negligible. The nitrile is instead heated with either a dilute acid such as dilute hydrochloric acid, or with an alkali such as sodium hydroxide solution. The end result is similar in all the cases, but the exact nature of the final product varies depending on the conditions you use for the reaction. Acidic hydrolysis of nitriles The nitrile is heated under reflux with dilute hydrochloric...

HYDROLYSING ESTERS

HYDROLYSING ESTERS This page describes ways of hydrolysing esters - splitting them into carboxylic acids (or their salts) and alcohols by the action of water, dilute acid or dilute alkali. It starts by looking at the hydrolysis of simple esters like ethyl ethanoate, and goes on to look at hydrolysing bigger, more complicated ones to make soap. Hydrolysing simple esters What is hydrolysis? Technically, hydrolysis is a reaction with water. That is exactly what happens when esters are hydrolysed by water or by dilute acids such as dilute hydrochloric acid. The alkaline hydrolysis of esters actually involves reaction with hydroxide ions, but the overall result is so similar that it is lumped together with the other two. Hydrolysis using water or dilute acid The reaction with pure water is so slow that it is never used. The reaction is catalysed by dilute acid, and so the ester is heated under reflux with a dilute acid like dilute ...

HYDROLYSING AMIDES

This page describes the hydrolysis of amides under both acidic and alkaline conditions. It also describes the use of alkaline hydrolysis in testing for amides. The hydrolysis of amides What is hydrolysis? Technically, hydrolysis is a reaction with water. That is exactly what happens when amides are hydrolysed in the presence of dilute acids such as dilute hydrochloric acid. The acid acts as a catalyst for the reaction between the amide and water. The alkaline hydrolysis of amides actually involves reaction with hydroxide ions, but the result is similar enough that it is still classed as hydrolysis. Hydrolysis under acidic conditions Taking ethanamide as a typical amide: If ethanamide is heated with a dilute acid (such as dilute hydrochloric acid), ethanoic acid is formed together with ammonium ions. So, if you were using hydrochloric acid, the final solution would contain ammonium chloride and ethanoic acid. ...

ESTERIFICATION

This page looks at esterification - mainly the reaction between alcohols and carboxylic acids to make esters. It also looks briefly at making esters from the reactions between acyl chlorides (acid chlorides) and alcohols, and between acid anhydrides and alcohols. What are esters? Esters are derived from carboxylic acids. A carboxylic acid contains the -COOH group, and in an ester the hydrogen in this group is replaced by a hydrocarbon group of some kind. We shall just be looking at cases where it is replaced by an alkyl group, but it could equally well be an aryl group (one based on a benzene ring). A common ester - ethyl ethanoate The most commonly discussed ester is ethyl ethanoate. In this case, the hydrogen in the -COOH group has been replaced by an ethyl group. The formula for ethyl ethanoate is: Notice that the ester is named the oppo...