A2 Chemistry 2021 Flashcards
What is the bond angle in benzene
120
Why is benzene more stable than triene
Benzene has delocalised electrons in a pi system which are spread out, minimising repulsion.
What is the difference in energy required to react between benzene and triene called
Resonance energy
Reagents and conditions for nitration
Conc HNO3, Conc H2SO4, 50*C
What are uses of the products of nitration
Used to make TNT or dyes.
Reagents and conditions for Friedel-Crafts reaction
Acyl Chloride, AlCl3, Anhydrous
What is the electrophile in Friedel-crafts reaction
RCO+ (acylium ion)
Reagents and conditions for Halogenation
AlCl3 or FeCl3 catalyst, Anhydrous
Reagents and conditions for alkylation
AlCl3 or FeCl3 catalyst, Anhydrous
Why is phenol a weak acid
The electrons from the oxygen atom get delocalised into the pi system of the benzene ring, making the phenoxide ion more stable.
What is the difference between an aromatic alcohol and phenol
The oxygen atom in phenol is bonded directly to the benzene ring.
Reagents and conditions for diazotisation
Phenylamine, HNO2 or NaNO2, HCl, <10*C
4 stages to make phenol from benzene
1) Nitration
2) Reduction
3) Diazotisation
4) Substitution
What is formed when phenol reacts with sodium
Sodium Phenoxide ion, Hydrogen gas
Why does Br attach to the 2,4,6 positions on phenol
As the -OH group is electron releasing, it increases the electron density in the 2,4,6 positions
Reagents and conditions for nitration of phenol
Dilute HNO3, Room temp
How is acyl chloride formed
By adding PCl5, PCl3, SOCl2 to carboxylic acids.
What is formed when PCl5 reacts with carboxylic acids
POCl3 + HCl
What is formed when PCl3 reacts with carboxylic acids
H3PO4
What is formed when SOCl2 reacts with carboxylic acids
SO2 + HCl
Why do acyl chlorides have high B.p
C-Cl bond has permanent dipole due to polarity
Reagents and conditions for making amines from halogenoalkanes
Halogenoalkane + Hot, Ethanolic NH3
Why is Hot ethanolic NH3 used to make amines
To prevent the formation of 2* or 3* amines
Reagents and conditions for making amines from nitriles
Step 1: KCN/HCN in ethanol, heated under reflux with halogenoalkane
Step 2: Hydrogen with Ni catalyst, pass vapours over dry ether
What is observed when phenylamide is added to bromine water
Bromine water decolourises and a white precipitate is formed
Why are amines good bases
The nitrogen atom has a lone pair of electrons available to bond with a H+ ion
Why is ammonia not basic
The nitrogen atom does not have a lone pair of electrons available to bond with H+
Reagents for triiodomethane reaction
Aqueous alkaline Iodine, NaOH
Why must diazotisation be done at <10*C
The diazonium ion formed is very reactive
Which position does coupling usually occur in
4
What is reacted to form nitrous acid
NaNO2, HCl
When azo compounds are formed why do they always join in the 4 position
Phenol is a ring activating group
Why are amides pH neutral
The lone pair of electrons from the nitrogen are delocalised alongside the electrons from the oxygen, making the ability to attract H+ non-existent
What is reacted to form amides
Acyl chlorides with amines
What is formed when HCl is reacted with excess ammonia
NH4Cl
What is reacted with amides to form amines
LiAlH4
What is formed by the reaction of amides with acids
- Carboxylic acids
- Ammonium or RNH3+ ions
What is formed by the reaction of amides with bases
- Acid salts
- Amines/Ammonia
What is the bond between amino acids called
Peptide bond
What is reacted to form amino acids
Amine + Carboxylic acid
What is formed form the reaction between Amine + carboxylic acid
Amino acids
What is a zwitterion
Amino acid with H moved from O to N;
-ve charge on O, +ve charge on N
Do elements with higher E* value get oxidised or reduces more easily
Reduced
On which side of the cell does the more positive electrode go
Right side
How do you know if an electrolysis reaction is feasible
The emf value (RHS-LHS) is positive
At the positive electrode, which side of the half equation does the equilibrium sit
Left
What is the name for two combined half cells
Electrochemical cell