Naming molecules/organic chem Flashcards

1
Q

Organic chemistry

A

Study of carbon and its many carbons

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2
Q

Why can carbon form many different compounds (allotropes)

A

Has 4 electrons in outer shell meaning it can form covalent bonds with four different atoms

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3
Q

Why are hydrocarbons good fuels

A

Only has hydrogen and carbon atoms, Make good fuels due to their covalent bonds which store a large amount of energy

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4
Q

What happens in a reaction of oxygen and hydrocarbons

A

releases CO2, H20 (gas), and energy (exothermic), in a limited supply of oxygen releases CO and H20 (gas)(incomplete combustion reaction)

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5
Q

Homologous series

A

Differs by -CH2- from previous member, have similar structure, chemical properties and general formula, have a pattern to their physical properties

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6
Q

Structural isomers

A

Occurs in alkanes that have 4+ carbon atoms, Same molecular formula but different arrangement of atoms

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7
Q

Parent chain

A

Longest continuous chain of carbon,number of carbons in parent chain= prefix

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8
Q

Substituent groups

A

Atoms or groups other than hydrogen on the molecule

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9
Q

Alkanes

A

Only single bonds, saturated hydrocarbons, non-polar, usually follows formula of CnH2n+2

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10
Q

Bonding in alkanes

A

Strong covalent bonds that increase as the size of the molecule increases meaning it has a high melting and boiling point in larger molecules, Weak intermolecular forces meaning lower melting and boiling point in smaller molecules, dispersion forces increase as mass of molecule increases

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11
Q

Alkenes

A

At least one double bond, usually follows formula of CnH2n

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12
Q

Cis-trans (geometric) isomers of alkenes

A

Joined in same arrangement but have a different arrangement in space due to the double bond between two atoms which keeps them in a fixed position, Two atoms joined by a single bond can rotate freely around the bond

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13
Q

Cis isomers

A

same group on each carbon is located on the same side of the double bond

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14
Q

Trans isomers

A

same group on each carbon is located on opposite sides of the double bond

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15
Q

Properties of alkanes (7)

A

Colorless, Low density, Non-polar (no charge), Insoluble in water, Low melting and boiling point, Mostly inert but can react with halogens in UV light, Combust easily (exothermic)

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16
Q

How do you test for alkenes/alkanes

A

Use bromine solution, alkanes will have no change in colour, alkenes will decolorise the solution

17
Q

Properties of alkenes (7)

A

Colourless, Non-polar (no charge), Insoluble in water, Low melting and boiling points, More reactive, Undergo addition reactions, Combust easily

18
Q

Addition reactions

A

occurs in alkenes where the double bond is broken and other atoms are added on, can be done with: hydrogen, halogens, hydrogen halides and water

19
Q

Benzenes (4)

A

C6H6- 6 carbon atoms joined in a ring each bonded to 1 hydrogen atom, Stable as the bonds are of equal strength, Have delocalised electrons which move through the ring, Aromatic- have sweet, pleasant aroma’s

20
Q

Properties of benzenes

A

Colourless liquid, Aromatic odour, Density is less than water, Non polar, Insoluble in water, Toxic, Volatile and high flammable, Combust with a black sooty flame

21
Q

Substitution reactions

A

Alkanes and benzenes react with halogens in UV light, Halogen atom replaces a hydrogen atom, if there is excess halogen further substitution may take place, Reaction can continue until all hydrogens have been substituted

22
Q

Saturated

A

can’t add anymore hydrogens as there are only single bonded, alkanes

23
Q

Unsaturated

A

can add more hydrogens by breaking double bond, alkenes