Question 1
Question
What shape is a sp3 hybridised C?
Answer
-
Tetrahedral
-
Trigonal planar
-
Linear
Question 2
Question
What shape is a sp2 hybridised C
Answer
-
Tetrahedral
-
Trigonal planar
-
Linear
Question 3
Question
What shape is a sp hybridised C
Answer
-
Tetrahedral
-
Trigonal planar
-
Linear
Question 4
Question
Alkanes are unsaturated hydrocarbons. True or false?
Question 5
Question
Alkenes are [blank_start]more[blank_end] reactive than alkanes because the delocalised electrons make them susceptible to attack by electrophiles.
Question 6
Question
Alkenes undergo [blank_start]electrophilic addition reactions[blank_end]
Question 7
Question
Alkynes are [blank_start]less[blank_end] reactive than alkenes.
Question 8
Answer
-
Substitution reactions
-
Electrophilic addition reactions but at a quicker rate than alkenes
-
Nucleophilic substitution reactions
-
Electrophilic addition reactions but at a slower rate than alkenes
Question 9
Question
Arenes are [blank_start]highly unsaturated[blank_end] and [blank_start]cyclic.[blank_end]
Answer
-
highly unsaturated
-
cyclic.
Question 10
Question
Arenas do not behave like alkenes and alkynes because they [blank_start]do not decolourise bromine water.[blank_end]
Question 11
Question
What type of molecule is benzene?
Answer
-
Trigonal planar
-
Planar
-
Linear
-
Tetrahedral
Question 12
Question
Benzene is a colourless liquid.
Question 13
Question
Boiling point of benzene?
Answer
-
90 degrees
-
100 degrees
-
70 degrees
-
80 degrees
Question 14
Question
Melting point of benzene
Answer
-
5.5 degrees
-
10 degrees
-
3 degrees
-
2.5 degrees
-
1 degrees
Question 15
Question
Label this drug molecule
Question 16
Question
Label this drug molecule
Question 17
Question
Label this drug molecule
Question 18
Question
The halogen atom on an alkylhalide atom is attached to what other atom?
Question 19
Question
The bond in alkylhalide are non-polar.
Question 20
Question
[blank_start]Cl-, Br- and I-[blank_end] are good leaving groups in nucleophilic substitution reactions.
Question 21
Question
Alkyl fluorides and fluorocarbons are relatively unstable.
Question 22
Question
Although the halogen-alkane bond is polar, they do not have a [blank_start]corresponding electron deficient region.[blank_end]
Question 23
Question
Although the halogen-alkane bond is polar, they do not [blank_start]interact strongly with water molecules.[blank_end]
Question 24
Question
Although the halogen-alkane bond is polar, they are generally _____
Answer
-
less lipophilic than corresponding non-halogenated molecules
-
more hydrophilic than corresponding non-halogenated molecules
-
more lipophilic than corresponding non-halogenated molecules
-
less hydrophilic than corresponding non-halogenated molecules
Question 25
Question
Tick all that is correct about halogens in drugs
Answer
-
Generally make the drug more lipophilic than corresponding non-halogenated molecules
-
Generally make the drug less lipophilic than corresponding non-halogenated molecules
-
Halogenated drugs are less readily metabolised than non-halogenated forms
-
Halogenated drugs are more readily metabolised than non-halogenated forms
Question 26
Question
Label this drug molecule
Question 27
Question
Tick all that is correct about DDT
Answer
-
Persistent in the environment
-
Chemically unstable
-
Chemically stable
-
Highly resistant to metabolism
-
Not very resistant to metabolism
Question 28
Question
Short-chain alcohols are [blank_start]freely miscible with water.[blank_end]
Question 29
Question
The interaction between short-chain alcohols and water can be explained [blank_start]by hydrogen bonding.[blank_end]
Question 30
Question
A permanent dipole exists in alcohol because of ...
Question 31
Question
R-OH dissociates to give [blank_start]R-O-[blank_end]
Question 32
Question
R-OH accepts a [blank_start]proton to give R-OH2+[blank_end]
Question 33
Question
Acidity of alcohols depends on the [blank_start]R-group[blank_end]
Question 34
Question
pKa is the [blank_start]negative log[blank_end] of acid dissociation constant
Question 35
Question
Acidity of molecule is increased if it has [blank_start]electron withdrawing group[blank_end] near the -OH group
Question 36
Question
Acidity of molecule is also dependent on if the rest of the molecule can [blank_start]stabilise the negative charge.[blank_end]
Question 37
Question
Phenols are [blank_start]stronger acids[blank_end] than alcohols.
Question 38
Question
Phenoxide ions are [blank_start]resonance stabilised.[blank_end]
Question 39
Question
What does the -OH functional group do and in what condition?
Question 40
Question
Relate the O- to the stability of the molecule
Question 41
Question
Fluorine is strongly electronegative.
Question 42
Question
The C-F bond in fluorine is polarised.
Question 43
Question
In fluorine, the partially positive charge on the carbon [blank_start]stabilises[blank_end] the negative charge on the hydroxyl group.
Question 44
Question
Tick all that is correct about the reactivity of phenols.
Question 45
Question
Contribution of alcohols to the properties of drugs: tick all that is correct about hydrogen bonding
Answer
-
Decreases the polarity of molecule
-
Increases the polarity of molecule
-
Adds to water solubility but generally not sufficient alone to ensure full water solubility
-
Ensures full water solubility
-
Involved in drug-target interactions as either a hydrogen bond donor or acceptor
Question 46
Question
Label this molecule
Question 47
Question
Label this molecule
Question 48
Question
Tick all this correct about ethers
Answer
-
Do not have hydrogen attached to the oxygen
-
Can be hydrogen bond donors
-
Can be hydrogen bond acceptors
-
Show full water solubility
-
Show partial water solubility
-
Solubility increases with chain length
-
Solubility decreases with chain length
Question 49
Question
Ethers can form [blank_start]peroxides in contact with air.[blank_end]
Question 50
Question
Ethers are generally non-reactive