C3 - Organic Chemistry Flashcards

0
Q

What is the general formula of an alcohol?

A

C and then subscript n

H and then subscript 2n + 1

Then OH

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1
Q

What is the functional group of alcohols?

A

-OH

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2
Q

What is the naming system for alcohols?

A

Replace the final “e” with “ol”

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3
Q

What would the chemical formula for propanol be?

A

C^3 H^7 OH

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4
Q

What are the 3 main chemical properties for most alcohols?

A

They burn in air to produce carbon dioxide and water

Dissolve completely in water to form neutral solutions

They react with sodium to give hydrogen and sodium ethoxide

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5
Q

What is the alcohol used in drinks and what is the problem with it?

A

Ethanol is used in drinks and it damages the liver and brain

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6
Q

How do you draw alcohols?

A
H    H  
       |     |    
H - C - C - O - H 
       |     | 
      H    H 
For ethanol etc. 

The top and bottom H’s need to be moved one to the left

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7
Q

What other 2 things can alcohols be used for?

A

Solvent

Fuels

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8
Q

What is a solvent?

A

A chemical that can dissolve substances that water can’t dissolve

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9
Q

In what 2 contexts are alcohols used as solvents?

A

Ethanol is used as the solvent for perfumes and aftershave lotions

Methylated spirit is ethanol with other chemicals mixed with it and it’s used to clean paint brushes

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10
Q

In what 2 ways are alcohols used as fuels?

A

They are burned in spirit burners

They can be mixed with petrol for use in a car

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11
Q

What are the 4 advantages of using ethanol as a fuel?

A

No smell

Clean burning so no pollution

Some developing countries can ferment sugar from sugar canes to get ethanol

Sugar cane is a renewable source

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12
Q

How else can you produce alcohols?

A

An example would be ethene + water –> ethanol

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13
Q

What is the functional group of carboxylic acids?

A

-COOH

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14
Q

What is the naming system for carboxylic acids?

A

Replace the “e” with “oic acid”

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15
Q

How do you draw carboxylic acids?

A
H   H       O
       |     |       //
H - C - C - C 
       |     |       \ 
       H   H       OH 

For propanoic acid

16
Q

What is the general formula for a carboxylic acid?

A

C and then subscript n

H and then subscript 2n+1

Then COOH

17
Q

What are the 3 main ways that carboxylic acids react?

A

Ethanoic (example) acid + metal carbonate –> metal ethanoate + carbon dioxide + water

Dissolves in water to ionise, release H+ ions and make the solution acidic

Carboxylic acid + alcohol –> ester + water

18
Q

What is the problem with acidic solutions of carboxylic acids?

A

They are weak acids

19
Q

How are carboxylic acids made?

A

An example is butanol + oxygen –> butanoic acid + water

20
Q

What are the 5 uses of carboxylic acids?

A

Ethanoic acid can be dissolved in water to make vinegar

Citric acid is another carboxylic acid which is present in fruits

Soaps and detergents are made from carboxylic acids and long chain carbon atoms

Used to make eaters

Can be used as a solvent but it makes the solution acidic

21
Q

What is the functional group of esters?

22
Q

What is the naming system for esters?

A

The alcohol forms the first part and the carboxylic acid forms the second part

An example is: for methane and propanoic acid, the ester is methyl propanoate

23
Q

How are esters made?

A

Alcohol and carboxylic acids react in the presence of an acid catalyst (usually sulphuric) to form the ester and water

24
Q

How do you draw esters?

A
H   O
 |    //
 H - C - C      H    H
       |       \       |     |
         H    O - C - C - H 
                        |     | 
                      H    H 

For ethyl ethanoate

The top left part is the carboxylic acid part and the bottom right is the alcohol

The top line has been shifted to the right

25
Q

What is the main use of esters and why?

A

Used for flavourings and perfumes because they smell nice and are also volatile meaning that the evaporated molecules can be detected easily by smell receptors

26
Q

What is the other main use of esters?

A

Solvents for paint, ink, glue etc.

27
Q

What are the 4 disadvantages of esters?

A

Very flammable and this makes them dangerous

Don’t mix well with water and not very soluble

Some esters irritate mucous membranes in the nose and mouth

Some are toxic