reactions of alkenes Flashcards

1
Q

what occurs in a reaction of alkene

A

the double c-c bond breaks with each carbon in that bond forming a new bond to another element/molecule, each part of the other reactant forms a bond with each carbon in the double bond

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2
Q

what is an alcohol

A

contaions an -oh group known as a hydroxyl group, which replaces one hydrogen in the structure of an alkane

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3
Q

genmeral formula alcohols

A

CnH2n+1OH

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4
Q

what to remember when naming an alcohol

A

replace the suffix ‘an’ of the alkane with ‘ol’ and make sure the carbons are numbered from the end of the carbon chain that gives the lowest number to the OH group

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5
Q

solubility of alcohols

A

soluble in water as the OH gropup allows alcohol molecules to form hydrogen bonds with water molecules

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6
Q

polarity trend of alcohols

A

decreases as the molecule becomes larger because the length of the chain increases and more of the molecule is non-polar

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7
Q

boiling point of alcohols compared to hydrocarbons

A

have a much higher boiling point as the -oh group allows hydrogen bonding to occur between molecules and strengthens the intermolecular bonding, most alchols are liquid at room temp whereas hydrocarbons are gases

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8
Q

trend of boiling point in alcohols

A

increases as the size of the alcohol molecule increases due to an ioncrease in dispersion forces

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9
Q

how top name alcohols

A

name alkane as usual but then put a dash (-) the carbon number alcohol is bonded to (-) ‘ol’

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10
Q

combustion of alcohols

A

readily undergo combustion when reacting with oxygen to form CO2 and H2O

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11
Q

what are carboxylic acids

A

weak acids that are often present in food, giving it a sour taste, contain a carboxyl group (-COOH)

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12
Q

general formula carboxylic acid

A

CnH2n + 1 COOH

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13
Q

where are carboxylic acids found

A

some insect venoms, when food detiriorates,

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14
Q

how to name carboxylic acids

A

keep regular alkane name, then remove suffic “an” and replace with -oic acid

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15
Q

things to remeber when naming carboxylic acid

A

the carboxyl carbon can only occur on the end of the chain so is always carbon 1, the carbon is the carboxyl group is counted when naming the molecule

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16
Q

why are carboxylic acids acids

A

the elctrons are drawn away from the hydrogen atoms, allowing it to react with water to form H+ ions, so that the functional group can act as an acid

17
Q

why to carboxylic acids have the highest boiling points

A

a dimer of two carboxylic acid monomers form two hydrogen bonds

18
Q

what is an ester

A

often fragrent molecules that cosist of a carbonyl group (C double bonded to O) with a second oxygen bonded to the carbon atom to form -COO

19
Q

general formula esters

A

R - COO - R’, where R and R’ are alkyl groups that may or may not be the same

20
Q

how are esters formed

A

when carboxylic acids are heated with alohols in the presence of suphuric acid (catalyst)

21
Q

what occurs during esterfication

A

the ester functional group is fortmed from the carboxyl functional group of the carbopxylic acid and the hydroxyl group of the alcohol, water is also produced

22
Q

process of drawing ester reaction

A
  1. draw the structure of the reactants with the carboxyl group and Oh GROUP NEXT TPO EACH OTHER 2. identify the atoms in the reactants that will form the water bmolecule 3. draw the remaining structure of the ester
23
Q

how to name esters

A

locate the functional group and carbonyl carbon 2. starting from the carbon in the functional group, determine the number of the carbons in the chain attached to it 3. name it according to the stem name, adding the suffic -oate (dervied from the carbopxylic acid) 4. the alkyl gropup bonded to the singly bonded oxygen atom is the front of the name (dervied from the alcohol)

24
Q

boiling point of esters

A

lower boiling points than alcohols or carboxylic acids as they have no free hydroxyl groups so cannot form hydrogen bonds with each other

25
Q

polarity of esters

A

polar but dont form hydrogen boinds