chapter 23 reactions in organic chemistry Flashcards

1
Q

substitution reaction

A

chemical reaction in which an atom/ group of atoms in a molecule is replaced by another atom/group of atoms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

mechanism

A

of a reaction is the detailed step by step description of how the overall reaction occurs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

why do chemists need the knowledge of the

mechanisms ?

A

in order to establish the best conditions for a particular reaction , hence maximise the yield of products (eg ; reaction nitrogen + hydrogen = ammonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

4 steps of a mechanism

A

initiation, propagation 1 , propagation 2 , termination

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

(methane + chlorine reaction ) Initiation (step 1 )

A

UV light provides the energy to split (homolysis) the chlorine bonds into chlorine free radicals

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

homolysis / homolytic fission

A

a chemical bond dissociation of a neutral molecule generating two free radicals

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

photo chemical reaction

A

reaction that is brought about by light

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

(methane + chlorine reaction ) Propagation (step 2)

A

chlorine atom attacks a (m)ethane atom to create hydrogen chloride and a species called (m)ethyl free radical

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

(methane + chlorine reaction ) Propagation (step 3)

A

(m)ethyl free radical attacks a chlorine molecule to form mono chloro (m)ethane and a chlorine free radical atom

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

chain reaction

A

reaction that continues on and on because a product from one step of the reaction is a reactant for another step of the reaction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

(methane + chlorine reaction ) Termination (step 4)

A

a no. of reactions takes place to stop the chain reaction (form molecules ; chlorine , chloro(m)ethane , ethane/butane

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

chlorination of methane

A

free radical substitution reaction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

reaction takes place when exposed to UV light [evidence]

A

the effect of UV light suggests homolysis (free radical mechanism) of Chlorine molecule to form 2 chlorine free radicals

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

for every photon absorbed thousands of chloro-(m)ethane molecules are formed [evidence]

A

this suggests a chain reaction is taking place

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

ethane/butane is found in the products

A

(m)ethyl free radicals must be present , 2 methyl free radicals combine to form ethane / 2 ethyl free radicals combine to form butane

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

adding a source of free radicals (tetra methyl lead) speeds up reaction

A

only a mechanism involving free radicals would be affected by adding a substance that provides free radicals

17
Q

addition of an inhibitor (oxygen ) slows down the reaction rate

A

this implies a chain reaction is taking place ( the inhibitor is combining with the free radicals to stop the chain formation

18
Q

uses of fully halogenated alkanes

A

flame retardants ( discontinued use because of the damage they do to the ozone layer )

19
Q

hydrolysis

A

the chemical breakdown of a compound due to reaction with water

20
Q

saponification =

A

base catalyzed hydrolysis of esters

21
Q

saponification formed by

A

ester + base = acid + alcohol