It’s not just WHAT you know, it’s HOW you write it!
I know, you’re studying Chemistry not English Lit but the one thing that sets A* grade students apart from the
Continue readingIt’s not just WHAT you know, it’s HOW you write it!
The ultimate A level chemistry resource
I know, you’re studying Chemistry not English Lit but the one thing that sets A* grade students apart from the
Continue readingIt’s not just WHAT you know, it’s HOW you write it!
Nitrogen bonds with oxygen to from a number of oxides and oxyanions, the most common of which are listed below
Continue readingBonding in the nitrogen oxides and oxyanions
The trend in the bonding and structure of the Period 3 oxides can be explained in terms of the increasing
Atomic radius Dedicated post explaining the trend in atomic radius is right here! Melting points and structure The melting point
Before we jump straight in, we really need to define how we measure the radius of an atom … This
Continue readingExplaining the trend in atomic radius across Period 3
Acyl chlorides and acid anhydrides are both more reactive than carboxylic acids, reacting with a wide range of nucleophiles and
Continue readingThe reactions of acyl chlorides and acid anhydrides
Making esters Esters are a derivative of carboxylic acids and formed from the reaction between a carboxylic acid and an
Carboxylic acids are weak organic acids. All acids are proton donors and the more stable the resulting anion (in this
Carboxylic acids contain the carboxyl functional group, -COOH, which is itself made from a carbonyl group and a hydroxyl group.
Continue readingNaming carboxylic acids and their derivatives
Aldehydes and ketones are examples of carbonyl compounds. In an aldehyde the carbonyl group, C=O, is bonded to at least