C10 - Organic Reactions Flashcards

1
Q

What do organic compounds form the basis of?

A

All living things

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2
Q

What atoms do all organic molecules contain?

A

Carbon atoms.

Carbon atoms form the backbone of all organic molecules.

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3
Q

What is a ‘functional group’?

A

The area of a molecule that is reactive and gives a ‘family’ of organic molecules its distinctive reaction characteristics.

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4
Q

What is the functional group in alkenes?

A

The ‘C==C’ double carbon bond.

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5
Q

What do chemists call a ‘family’ of organic compounds with the same functional group?

A

A homologous series.

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6
Q

What are some examples of homologous series?

A

Alkanes - Methane, Ethane, Propane, Butane, Pentane

Alkenes - Ethene, Propene, Butene, Pentene

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7
Q

Why are Alkenes very reactive?

A

Because of the ‘C==C’ double carbon bond.

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8
Q

Why are Alkenes rarely burned?

A

Alkenes release far less energy than alkanes.

Alkenes tend to undergo incomplete combustion - so they burn with a smoky flame.

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9
Q

What are alkenes useful for making/producing?

A

Alkenes are so valuable in making polymers and plastics.

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10
Q

What type of reaction do alkenes undergo?

A

Addition Reactions

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11
Q

What happens in an addition reaction of an alkene?

A

The C==C double carbon bond undergoes the addition.

The C=C double carbon bond becomes a single C–C bond, and other atoms join onto the 2 carbon atoms.

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12
Q

What is the general formula/template for an addition reaction?

A

General Formula:
X Y
| | | |
C==C + X—Y —> —C—C—
| | | |

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13
Q

How do alkenes react with the halogens? (C2, Br2, I2) Give an example:

A
  • The C==C double bond becomes a single bond.
  • The number of hydrogen atoms stays the same.
  • The 2 halogen atoms are added on to the displayed formula.

Example:

Ethene + Bromine —> *Dibromoethane

C2H4 + Br2 —> C2H4Br2

*Dibromoethane is colourless because of the presence of bromine (think about alkene test in orange coloured bromine water).

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14
Q

How do alkenes react with hydrogen, (H2)? What conditions must the reaction be under? Give an example:

A

-Alkenes react with hydrogen (H2) to produce an alkane - due to the fact that the maximum number of hydrogen atoms are now attached.

Conditions:
-The reaction must be at a temperature of 150°C with a NICKEL CATALYST.

-This process of hydrogenising alkenes is used to make margarine.

Example:

Ethene + Hydrogen —> Ethane

C2H4 + H2 —> C2H6

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15
Q

How do alkenes react with water (steam)? What conditions must the reaction be under? Give an example:

A

-Alkenes make alcohols when reacted with water (steam).

Conditions:
-There must be a high temperature and a concentrated PHOSPHORIC ACID CATALYST.

  • Displayed Formula:
  • The alkene gains 2H’s and an O (H2O) from the water. So you draw an O—H as well as an H on its own, onto the hydrocarbon.

Example:

Ethene + Steam —> Ethanol

C2H4 + H2O —> C2H5OH

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16
Q

What functional group does the homologous series of alcohols contain?

A

The ‘OH’ functional group.

This helps you to recognise an alcohol.

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17
Q

What is the general formula for an alcohol?

A

(CnH2n+1)OH

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18
Q

What are the the first 4 alcohols and there chemical formula?

A

Methanol, CH3OH
Ethanol, C2H5OH
Propanol, C3H7OH
Butanol, C4H9OH

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19
Q

Which alcohol is ‘common alcohol’ used in drinks?

A

Ethanol, C2H5OH

20
Q

What does the displayed formula of an alcohol look like?

A

It looks like a hydrocarbon except on one of the branches, there is an O connected to an H:

Methanol:

         H
         | 
H — C — OH
         |
         H
21
Q

What molecules are alcohols definitely not examples of?

A

They are NOT Hydrocarbons.

They don’t have just hydrogen and carbon atoms in their bonds.

22
Q

What functional group does the homologous series of carboxylic acids contain?

A

The ‘COOH’ functional group.

23
Q

What is the general formula for carboxylic acids?

A

Cn-1H2n-1COOH (or CnH2nO2)

E.g Ethanoic Acid = 1C, 3H + COOH gives you CH3COOH.

24
Q

What are the first 4 carboxylic acids and what are there chemical formulas?

A

Methanoic Acid, HCOOH (CH2O2)

Ethanoic Acid, CH3COOH

Propanoic Acid, CH3CH2COOH

Butanoic Acid, CH3CH2CH2COOH

*Essentially you start with HCOOH (CH2O2), and you add CH3. Then you add CH2 each time.

25
What carboxylic acid is the main acid in vinegar?
Ethanoic Acid, CH3COOH
26
What is an Ester? How is an Ester formed?
An Ester is a chemical compound derived from an acid. An Ester is formed if you replace the H in the 'COOH' of a carboxylic acid with a hydrocarbon.
27
What functional group does an Ester contain?
The 'COO' functional group.
28
What is one example of an Ester?
Ethyl Ethanoate, CH3COOCH2CH3 (C4H8O2)
29
How do you draw the displayed formula of ethyl ethanoate?
The chemical formula is CH3COOCH2CH3. Move from left to right. ``` H | H — C — C == O H H | \ | | H O — C — C — H | | H H ``` Here you can see methane (CH3), connected to a (COO) which then branches off with a (CH2) and a (CH3).
30
What are the 2 methods of making common alcohol (ethanol)?
1) Industry: Reacting ethene with steam (+ a phosphoric acid catalyst). 2) Lab: Fermenting sugars (e.g glucose) from plants with yeast: C6H12O6 (+yeast catalyst) —> 2C2H5OH + 2CO2
31
How does ethanol (common alcohol) burn/combust? What do alcohols burning produce?
Ethanol burns completely and well in air with a 'clean blue flame'. (Think christmas pudding), and produces Carbon Dioxide and Water. Ethanol + Oxygen —> Carbon Dioxide and Water C2H5OH + 3O2 —> 2CO2 + 3H2O *This is oxidation by combustion.
32
How can the combustion of ethanol be used?
Ethanol can be used as an alternative fuel to petrol and diesel. It is classed as a type of BIOFUEL.
33
How do alcohols react with sodium?
When an alcohol reacts with sodium metal, it forms a solution of: - a sodium alkoxide (e.g sodium methoxide/sodium ethoxide) - hydrogen gas E.g Sodium + Ethanol —> Sodium Ethanoxide + Hydrogen The solution effervesces (fizzes/gives off bubbles) as hydrogen is produced.
34
How can ethanol be chemically oxidised (without burning)? What products are formed? How do they compare to the products from oxidation by combustion?
Alcohols can be chemically oxidised by: 1) CONTROLLED (naturally occuring) - reacting with chemical oxidising agents 2) UNCONTROLLED - reacting with microbes in the air. The process produces ethanoaic acid (main acid in vinegar) and water. E.g Ethanol + Oxidising Agents —> Ethanoic Acid + Water (don't need to know symbol equation). *These products are different oxidation products compared to oxidation from combusting.
35
What are the 3 main uses of alchohols?
1) Fuels - ethanol used as a biofuel. 2) Solvents - perfumes, mouthwashes, aftershaves and cleaning products. Evaporates quicker than water. (lower boiling point). 3) Drinks - ethanol is used, all acohols are toxic but ethanol is the least toxic and can be metabolised by enzymes. (If you drank methanol, propanol or butanol - you could easily die).
36
What pH range do solutions of carboxylic acids have?
Less than 7 (all acidic).
37
Do carboxylic acids have the same typical reactions as other acids?
Yes
38
How do carboxylic acids react with metal carbonates? *Think CAWCS
Metal Carbonate + (carboxylic) Acid —> Water + Carbon Dioxide + Salt E.g Sodium Carbonate + Ethanoic Acid —> Water + Carbon Dioxide + Sodium ethanoate (salt)
39
What is the main observation for a reaction between a metal carbonate and a carboxylic acid?
Fizzing as CO2 is given off.
40
What type of acid is a carboxylic acid? Strong or Weak
Weak Acid Acids like HCl are strong.
41
How are acids determined as strong or weak? How do strong acids react with water VS weak acids?
By their reactions with water. Strong acids: All acid molecules break down to form H+ Ions, causing violent fizzing. Weak acids: ONLY A FRACTION of the molecules break down to form H+ ions, causing less violent fizzing. General Formula: Acid + Water —> H+ ions
42
How would the pH value of a strong and weak acid aqueous solutions compare with the same concentration?
Weak acids would have a higher pH in the same concentration as they are less acidic and therefore contain less H+ ions. *the acids are aqueous so they will always contain H+ ions. Strong = all molecules break down to form H+ ions. Weak = some of molecules break down to form H+ ions.
43
How are esters made? What is the general formula for making an Ester?
Esters are made by reacting a carboxylic acid with an alcohol (in the presence of a sulfuric acid catalyst). Water is also produced. Formula: Carboxylic Acid + Alcohol (with catalyst) ⇌ Ester + Water The reaction is reversible.
44
What are the properties of Esters?
Esters are: - volatile (turn into a gas / vapourises easily) - fragrant - many smell sweet and fruity.
45
How are esters used based on their properties?
Used as perfumes, fragrances and food flavourings (pears, strawberries, oranges, rasberries, bananas, apples and pineapple all contain esters).