F324 part 1 Flashcards
(46 cards)
Short hand notation for a fatty acid
A:B(C)
A = number of carbon bonds
B = number of double bonds
C = position(s) of double bonds
Equation for benzene reacting with chlorine
C6H6 + Cl2 –> C6H5Cl + HCl
Conditions for nitration of benzene
Conc. nitric acid, conc. sulphuric acid, 50ºC
Reaction of phenol and potassium hydroxide and organic product formed
C6H5OH + KOH –> C6H5O-K+ +H2O
Potassium phenoxide
3 common amines and short description
Amphetamine: treats daytime drowsiness and chronic fatigue syndrome
Phenylephrine: decongestant, in cold and flu medicine
Adrenaline: flight or fight hormone
Equation for propan-1-ol being fully oxidised
C3H7OH + 2[O] –(K2Cr2O7/H2SO4)–> C2H5COOH + H2O
heated under reflux
What reducing agent is used in the reduction of carbonyls
NaBH4
Observations for reaction of phenol with bromine
Bromine decolourises, white preciptate forms (2,4,6- tribromophenol)
Equation for ethanoic anhydride with methanol
(Ch3CO)2O + CH3OH –> CH3COOCH3 + Ch3COOH
Conditions for acid hydrolysis of esters
Heated under reflux with dilute sulphuric acid or dilute hydrochloric acid
Condition for oxidising primary alcohol to aldehyde
Distillation (prevents further reaction)
Name of product formed from bromine and cyclohexene
1,2- dibromocyclohexane
What is a nucleophile
An atom or group of atoms attracted for an electron deficient centre where it donates a pair of electrons, forming a covalent bond
Shape and bond angles around a carbon atom in a benzene ring
Triginal planar, 120º
Observation seen by acidified dichromate ions (colour change)
Orange to green
Product produced in the bromination of phenol
2,4,6- tribromophenol
How to identify a specific carbonyl compound
React with 2,4- DNPH, filter and recrystallise precipitate(purify), determine melting point and compare against known values
Observations of melted phenol and potassium
Potassium disappears, effervescence
Two ways to make esters
From carboxylic acids
From acid anydrides
Chemical test for an aldehyde/ Ketone and its observation
Brady’s reagent (2,4- DNPH) orange precipitate
Why does alcohol dissolve in water?
Hydrogen bonds form between the polar OH grouop and water molecules
Why does benzene react with substitution reactions rather than addition reactions?
Subsition maintains the stability of the benzene ring. The product from an addition reaction would be less stable because the delocalisation in the ring structure would be lost
Reaction of methylamine as a base
Ch3H2N: + H^+ —> [H3CNH3}^+
How to differentiate between an aldehyde and a ketone, with observations
Tollen’s reagent:
Aldehye- forms silver grey solid, ‘silver mirror’
Ketone- no reaction