Unit 12 - Organic Chem Flashcards

(37 cards)

1
Q

specialities of carbon which allows to form multiple bonds

A

it is Tetravalent which means it can gain lose or share electrons

Its catenation is that it can form single, double or triple bonds

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2
Q

3 types of chains of carbon which can be found in compounds?

A

Straight Chain
Branched Chain
Closed chain

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3
Q

Hydrocarbons and their types?

A

Compounds contianing only hydrogen and carbon

  1. Saturated hydrocarbons where there is a carbon-carbon single bond such as Alkane, Alkyl and Alcohol
  2. Unsaturated hydrocarbons where there is only one carbon-carbon double or triple bond and rest all are single bonds. Such as alkyne and alkene
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4
Q

members of the same homologus series are…

A

differ by CH2
Have same functional group
tend to react similarly

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5
Q

IUPAC nomenclature form for hydrocarbons

A

Prefix + Word Root + Primary suffix + Secondary suffix

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6
Q

Word root in IUPAC nomelcautre

A

Longest continous chain of carbon atomd

1 = meth
2 = eth
3= prop
4 = but
5 = pent
6 = hex
7= hept
8 = oct
9 = non
10 = dec

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7
Q

Primary suffix in IUPAC Nomelclature

A

Determines if compound is saturated or not

Carbon-carbon single bond = ane
Carbon-carbon double bond = ene
carbon - carbon triple bond = yne

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8
Q

Prefix in IUPAC nomeclature

A

fluoro (-F)
chloro (-Cl)
bromo (-Br)
iodo (-I)
nitro (-NO2)
alkyl group (-R)

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9
Q

Alkane, formula and name of first 5 compounds

A

Formula = C_n H_2n+2

Saturated and all bonds between carbon are single bonds. Primary suffix = ane

First 5 elements = Methane, Ethane, Propone, Butane, Pentane

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10
Q

Alkene, formula, name of frist 5 compounds

A

C_n H_2n

One carbon-carbon bond will be a double bond rest all are single bonds. Unsaturated meaing we can break the double bond to add hydrogen. Primary Suffix = ene

First 5 = Ethene, Propene, Butene, Pentene, Hexene

Starts with eth and not meth because we need 2 carbons to make a double bond

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11
Q

Alkyne, formula and name of first 5 compounds

A

C_n H_2n-2

One carbon-carbon trple bond rest all are single bonds. Unsaturated. Primary Suffix = yne

first 5 compounds = ethyne, propyne, butyne, pentyne, hexyne

Starts with eth and not meth because we need 2 carbons to make a triple bond

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12
Q

Alkyl, formula and name of first 5 compounds

A

C_n H_2n+1

Remove one hydrogen from alkane to get alkyl. Primarry suffix = yl
Represented using ‘R’
Cant exist alone and will always be connected to a compounds

First 5 = methyl, ethyl, propyl, butyl, pentyl

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13
Q

Alcohol, formula and name of first 5 compounds

A

C_n H_2n+1 OH

Basically an Alkyl group with a OH (hydroxyl)
Suffix = ‘ol’
Weak acids’
Saturated hence mainly carbon-carbon single bond.
A number in front of the ‘ol’ suffix indiciated the position of the OH, for example, Propan-2-ol means the OH is bonded with the second carbon

First 5 - methanol, ethanol, propanol, butanol, pentanol

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14
Q

Hydration reaction

A

Adding water to alkene, in the prescene of heat and concentrated H2SO4 will give you an alcohol.

In the alkene, the carbon atom with most directly connected hydrogens will gain a single hydrogen from water (because the double bond breaks and one space for hydrogen comes up) and the cabron with least hydrogen directly connected often gets the OH from water

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15
Q

Carboxylic Acid, egenral form and name of first 5

A

O.
||
R - C - OH

Functional group = COOH
Suffix = anoic acid
Very weak acid with partial dissassociate of ions

Seires - Methanoic Acid, Ethanoic Acid, Propanoic acid, Butanoic acid, pentanoic acid

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16
Q

Why is the first compound in Carboxylic sereies HCOOH and not CH_3COOH?

A

Because for the first one, the longest chain of carbons should be oen and one cabron is already present in COOH, hence we consider the Alykyl group R to be just a Hydrogen

17
Q

Ionisation of Carboxylic acids

A

Carboxylic acid diassociates partially and loses the H at the end of COOH, to form a negative ion which always ends in ‘anoate’ and gives at an H+ ion

Other reactions are normal reaction of an acid with metal, base and metal carbonate

18
Q

Carboxylic acid reaction with water

A

Carboxylic acid + H2O ⇌ Carboxylate Ion + H_3 O+

19
Q

How is carboxylic acid formed?

A

By oxidising alcohol.

It can be doen using a Reflex Condenser in the prescene of Oxidisng agent such as Concentrated Sulphuric Acid (H2SO4) or Pottasium Dichromate (K2 Cr2 O7).

20
Q

Esters, general form and uses and suffix and functional group

A

O
||
R - C - O- R’

R = can be a hydrogen or an alkyl group, treated as Word root
R’ = strictly an alkyl group, treated are the prefix due to bonding with oxygen

Functionla group of esters = COO
Suffix = anoate
Used are perfums
Isomers of carboxylic acids

21
Q

Formation of Ester, reaction and its description, and what is it also called as??

A

Known as esterification
Formed by reacting carboxylic acid and alcohool

Reaction:
Carboxylic Acid + Alcohol = Ester + Water

The hydrogen in Alcohol bonds with OH in carboxylic acid to form water, leaves behind a carboxylic acid which bonds with the single remaining oxygen atom in alcohol to form an ester

22
Q

Easy wat to name ester, from both diagram and reactin

A

from reaction:
1. Replace anol’’ with ‘yl’ of the alcohol used
2. Replace anoic acid with anoate of the carboxylic acid used
3. form the name using structure = Alcohol first and carboxylic acid second

From diagram:
Alkyl Carboxanoate
See the alkyl connected with single bond oxygen, put as prefix
The remaining, I.e the compound connected with the carbon and double bond oxygen, becomes the longest continuous chain + suffix of anoate

23
Q

Uses of Alkane and Alkene

A

Alkanes are often used as feuls due to their High energy output and efficient combustion. Examles includes LPG, petrol and diesel.

Alkene are used in making of Plastics and pharmaceuticals

24
Q

Trends of compounds in same homologus series (as we go down the grooup)

A
  1. C1 - C5 are gasoeus in State
    C6 - C12 liquid in state
    C13+ solid state
  2. BP increases
  3. Density increases
  4. Volitality or how long it takes a subtsnace ot turn into vapours decreases
25
Properties of Alkane
Very unreactive because of high bodn energy Can be used as a very good fuel Can undergo Substituition and Combustion reaction Can react under the prescene of UV light, Sunlight or Heat to undergo Photochemical reaction
26
Hydrogenation reaction
Adding H2 to an Alkene in the prescene of Nickel as a catalyst at 150 degrees celcius to obtain a Alkane Eg: Ethene + H2 -> Ethane
27
Electrophillic Addition reaction example - bromination
Orange coloured Bromine water is added to Alkene attacks its double bond and breaks them. To fill the valency, the bromine bonds with the carbon atoms. The orange coloured liquid now becomes colourless as bromine isnt just there on its own. This is used to identify wether a solution was an alkene or an alkane, as with an alkane, no change would have occured
28
what is addition reaction of bromine and alkene called
bromination
29
Isomers
2 or more organic compounds having the same molecular formula but have diff structures
30
Carboxylic acids and Esters are ____ of each other
Isomers
31
Polymerisation
Many monomers combining at hight temperatre and pressure to form polymers
32
Appartus to measure surface area
BET Surface Area Analyzer
33
Photchemical reaction of halogenation of chlroination of methane, reaction and final formula
Equ: CH4 + 4Cl2 = CCl4 + 4HCl We continue to add Cl2 under the prescene of UV light to break bonds with hydrogen and replace hydrogen with chlorine atom
34
What is the name of the functional group of alkane/alkene/alkyne with halogen
Halogenoalkane or ene or yne depending on what is used
35
oxidising agent used in oxidatin of alcohol
sodium dichromate (Na2Cr2O7)
36
combustion reaction with general form of reaction
Happens in prescne of heat, oxyegn and an organic substace to give out water, co2 reaction form: organic substance + O2 = CO2 + H2O
37
explain why some compounds with same molecular formula can be differenent and what are the known as ?
They may have same number and type of atoms, but their structural composition may be different these are called isomers