alkanes Flashcards

1
Q

explain the bond angle and shape around each carbon atom in an alkane

A

each carbon atom is surrounded by 4 electrons in sigma bonds. repulsion between these electrons results in a tetrahedral shape and 109.5 bond angle around each carbon atom

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2
Q

explain the variation in boiling points of alkanes in terms of chain length

A

as chain length increases, boiling point increases. this is because the london forces have more points of contact between molecules and so will be stronger, requiring more energy to overcome

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3
Q

explain the variation in boiling points of alkanes in terms of branching

A

as branching increases, boiling point decreases. this is because the branches prevent the molecules from getting as closely together and also decreases the points of contact between them, making the london forces weaker (therefore less energy required to overcome)

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4
Q

what is homolytic fission?

A

each bonding atom receives one electron from the bonding pair, forming two radicals

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5
Q

what is heterolytic fission?

A

one bonding atom receives both electrons from the bonding pair

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6
Q

define radical

A

a species with an unpaired electron

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7
Q

what symbol is used to represent radicals in curly arrow mechanisms?

A

dots

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8
Q

what does a curly arrow represent?

A

the movement of a pair of electrons, showing either heterolytic fission or the formation of a covalent bond

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9
Q

why do alkanes have low reactivity?

A

C-C and C-H bonds are non polar, and have a high bond enthalpy

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10
Q

what are the products of the complete combustion of an alkane?

A

carbon dioxide and water

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11
Q

what are the products of the incomplete combustion of an alkane?

A

carbon monoxide (CO) or carbon as soot, and water

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12
Q

why is carbon monoxide so dangerous?

A

it is colourless and odourless. it reacts irreversibly with haemoglobin to form carboxyhaemoglobin, which prevents the red blood cell from carrying oxygen around the body

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13
Q

what do alkanes need to react with halogens (chlorine and bromine)?

A

UV (ultraviolet) radiation

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14
Q

what are the limitations of free radical substitution in organic synthesis?

A

-further substitution
-substitution at different positions in a carbon chain e.g. pentane could form 3 different isomers (1-bromopentane, 2-bromopentane, 3-bromopentane)

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