Module 4 Flashcards
Electrophile
atom/group of atoms that is attracted to an electron-rich centre - accepts electron pair to form new covalent bond
Electrophilic Substitution
Substitution reaction where an electrophile is attracted to an electron-rich centre or atom, where it accepts a pair of electrons to form a new covalent bond
Reaction Mechanism
Series of steps that make up the overall reaction
REFLUX
Continuous evaporation and condensation to prevent volatile reagents escaping
Curley arrow
Movement of a pair of electrons
Phenol
-OH group directly bonded to a benzene ring
Uses of pheno
Producing plastics (polymers), antiseptics, disinfectants and resins for paints
How does an amine act as a base?
Ammonia has a lone pair of electrons on the nitrogen atom which can be donated to the proton forming a dative covalent bond - so has accepted the H+ proton
Aliphatic
Hydrocarbon group with carbons in a chain
Aromatic
Hydrocarbon group containing a benzene ring
Functional Group
Part of an organic molecule responsible for its reactions
Electronegativity
Measure of attraction of a bonded atom for the pair of electrons in a covalent bond
Aldehydes
Carbonyl group at start of chain
Ketones
Carbonyl group in middle of chain
Nucleophile
Atom/ group of atoms attracted to an electron-deficient centre, where it donates a pair of electrons to form a new covalent bond
Esterification
Reaction of an alcohol with a carboxylic acid to produce an ester + water in a condensation reaction
Hydrolysis
Reaction with water/OH- ions which breaks a chemical compound into two - reverse of esterification
Formation of an Acid Anhydride
Forms by removal of H2O molecule from two identical carboxylic acid molecules