Organic (3.3) Flashcards
(40 cards)
Why is cracking used?
-Low demand but high supply of long-chain hydrocarbons
-High demand but low supply of shorter-chain (especially naptha fraction)
Alkenes produced are much more reactive than naturally occurring alkanes, so better used as fuels
What is cracking?
Splitting up of longer-chain hydrocarbons to produce shorter chain hydrocarbons
What conditions are required for thermal cracking?
- 700-1200K
- 7000kPa
What are the products of thermal cracking?
- Alkanes & Alkenes (1:1)
- Formed through intermediate, highly reactive free radicals
What conditions are required for catalytic cracking?
- 720K
- Slight pressure
- Zeolite catalyst (honeycomb structure, aluminium oxide & silicon dioxide)
What are the products of catalytic cracking?
How are they separated?
- Branched alkanes
- Cycloalkanes
- Aromatic compounds
-Separated by fractional distillation
Describe features of fractional distillation
- Continuous process
- Large scale
- Multiple collection points
- Produces fractions (mixtures of similar bpts)
- Used to separate complex mixtures with close bpts)
Describe the features of simple distillation
- Batch process
- Small scale
- Single collection point
- Produces pure substances (single bpt)
- Used to separate simple mixtures with widely different bpts
What is isomerism?
Molecules with the same molecular formula, whose atoms are arranged differently
What is structural isomerism?
Molecules with the same molecular formula, with differing structural formulae
What is position isomerism?
(STRUCTURAL)
-The functional groups are the same but attached to the chain at differing points
What is functional group isomerism?
(STRUCTURAL)
-Same molecular formula but different functional groups
What is chain isomerism?
(STRUCTURAL)
- Same molecular formula but the chain is arranged differently
- (e.g. branching etc)
What is stereoisomerism?
Molecules have the same structural formula, but are arranged differently in space
What is geometric isomerism?
(STEREO)
- E-Z isomerism refers to the orientation of the largest molecules around a double bond
- E=different side
- Z=same side
How does geometric isomerism arise?
It arises due to restricted rotation about a double bond
What is optical isomerism?
(STEREO)
- Occurs when four different substituents are attached to one carbon atom (chiral carbon)
- Essentially a reflection (cannot be superimposed)
What is a racemic mixture?
- A racemic mixture is a 50:50 mix of two enantiomers
- Optically inactive as the enantiomers rotate the plane of polarization of polarised light oppositely
Why are racemic mixtures formed?
Racemic mixtures are formed as the likelihood of attack from above or below the planar centre is equal, creating two opposing forms of chiral molecules
What are the products of complete combustion?
-H2O & CO2
Describe the enthalpies of combustion reactions
- Combustion reactions give out large amounts of heat, and hence have large negative enthalpies
- The more carbons present, the greater the heat output, and the larger the negative enthalpy (but the harder they are to ignite)
- Heavily exothermic
What is a fuel?
- A substance that releases heat energy when it undergoes combustion
- One which stores a large amount of energy for a small weight
What is incomplete combustion?
-A combustion reaction that takes place in a limited supply of oxygen (not lack of)
What are the products of incomplete combustion?
- CO & H2O
- In even less oxygen: C (soot) & H2O