Topic 9- Introduction to Organic Chemistry Flashcards
What sort of bonds do carbon atoms form?
What three types of carbon-carbon bonds?
What are the three ways that carbon atoms can be arranged in?
What is the chemistry of an organic compound determined by?
What is the molecular formula?
What is the empirical formula?
What is the structural formula?
What is the displayed formula?
What is the skeletal formula?
What aren’t shown as symbols in the skeletal formula?
Strong covalent bonds to each other
Single, double or triple
- Straight chains
- Branched chains
- Rings
Its functional group
The exact number of atoms of each element present in the molecule
The simplest whole number ratio of atoms of each element in the molecule
The minimal detail using conventional groups, for an unambiguous structure
Shows both the relative placing of atoms and the number of bonds between them
Used to show a simplified organic formula by removing hydrogen atoms from alkyl chains leaving just a carbon skeleton and associated functional groups
The carbon atoms and the hydrogen’s attached to them aren’t shown as symbols.
What is the general formula?
What is a root?
What are the roots for the following number of carbons:
1
2
3
4
5
6
What are prefixes?
What are the side chains for the following prefixes:
Methyl
Ethyl
Propyl
Butyl
Pentyl
Hexyl
Represents any member of a homologous series
A systematic name has a root that tells us the longest unbranched hydrocarbon chain or ring
Meth-
Eth-
Prop-
But-
Pen-
Hex-
Added at the beginning of the root, for example, side chains whose names tells us the number of carbons
CH3-
C2H5-
C3H7-
C4H9-
C5H11-
C6H13-.
What are suffixes?
Give an example of a suffix?
What can functional groups consist of?
What does each functional group have (full detail)?
What is a homologous series?
What do all homologous series share the same?
What does the formula of a homologous differ from its neighbour by?
What do all members of homologous series contain?
What do all members of homologous series have that’s similar?
What gradual change is shown in a homologous series?
Added at the end of the root
For example, alcohols have the suffix -ol, as in ethanol (CH3 CH2 OH)
One atom, a group of atoms or multiple bonds between carbon atoms
Each functional group has its own distinctive properties which means that the properties of a compound are governed by the functional group (s) in it
A series of compounds of similar structure in which each member differs from the next by a common repeating unit, CH2
All share the same general formula
Formula of a homologue differs from its neighbour by CH2 (eg CH4, C2H6 etc)
Contain the same functional group
Have similar chemical properties
Show a gradual change in physical properties as molar mass increases.
What does a suffix show in a systematic name?
What are the two steps for a systemic name?
What are the suffixes for the following functional groups:
Alkane
Alkene
Alkyne
Alcohol
Aldehyde
Ketone
Acid
Why must be given in many cases to avoid ambiguity?
What are substituents?
What must be numbered in substituents?
An ending that tells you which functional group is present
- See if any functional groups are present
- Add relevant ending to the basic stem
- ANE
- ENE
- YNE
- OL
- AL
- ONE
- OIC ACID
In many cases the position of the functional group must be given to avoid any ambiguity
Many compounds have substituents (additional atoms, or groups) attached to the chain
Their position is numbered.
How are carbon based substituents named?
What is their prefixes and give an example?
How do you number the principle chain?
How do side chain names appear and give some examples?
What is each side chain given?
What happens if identical side chains appear more than once (full detail with examples)?
How are numbers separated from names by and give an example?
How are numbers separated from numbers by and give an example?
Carbon based substituents are named before the chain name
They have the prefix -yl added to the basic stem (eg CH3 is methyl)
Number the principle chain from one end to give the lowest numbers
Side chain names appear in alphabetical order (butyl, ethyl, methyl, propyl)
Each side chain is given its own number
If identical side chains appear more than once, prefix with di, tri, tetra, penta, hexa)
Numbers are separated from names by a hyphen (eg 2-methylheptane)
Numbers are separated from numbers by a comma (eg 2,3 - dimethylbutane).
What is not always the longest chain in alkenes?
What must alkenes contain?
What does the name of an alkene end in?
What is the position of an alkene counted from?
What is the position of an alkene indicated by?
What is the side chain of an alkene similar to?
What is the side chain position of an alkene based on?
In alkenes, the principle chain is not always the longest chain
Must contain the double bond
-ENE
Count from one end as with alkanes
Indicated by the lower numbered carbon atom on one end of the C=C bond
Side chain of an alkene similar to alkanes
Position is based on the number allocated to the double bond.
What is the definition of structural isomerism?
What are the four properties of chain structural isomerism?
What are the five properties of position structural isomerism?
What are the three properties of functional group structural isomerism?
What can sometimes occur in the same molecule?
What does it mean the more carbon atoms there are?
In nomenclature, which way do you count from?
What does the double bond do in nomenclature?
What does anything mean in the bracket mean?
Where can you never have a methyl group attached in a chain?
Compounds that have the same molecular formula but different structural formula
- Different arrangements of the carbon skeleton
- Similar chemical properties (same)
- Slightly different physical properties
- More branching= lower boiling point
- Same carbon skeleton
- Same functional group
- Functional group is in a different position
- Same chemical properties- slightly different physical properties
- Different functional group
- Different chemical properties
- Different physical properties
Sometimes more than one type of isomerism occurs in the same molecule
The greater the number of possible isomers
Left/right to count from depending on which side has the lowest number for the side chains
The double bond takes the lowest number
Anything in the bracket means attached to the carbon (not always just the side chains)
You can never have a methyl group attached to the first carbon in the chain.