4.1 Basic concepts & Hydrocarbons Flashcards

(47 cards)

1
Q

What’s a Homologous series?

A

substances in a series with the same functional group and successive members differ only by a CH2

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2
Q

What’s an Aliphatic hydrocarbon?

A

when carbons joined in either straight or branched chains

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3
Q

What’s an Alicyclic hydrocarbon?

A

when carbons joined in ring structure

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4
Q

What’s an Aromatic hydrocarbon?

A

when carbons joined with at least 1 benzene ring in the structure

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5
Q

What’s the difference between a saturated and unsaturated hydrocarbon?

A
Saturated= only single bonds
Unsaturated= contains at least 1 double bond
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6
Q

What’s a functional group?

A

group of atoms responsible for a characteristic reaction of a compound

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7
Q

What’s a General formula?

A

simplest algebraic formula for a homologous series

e.g Cn H2n+2

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8
Q

What’s a Displayed formula?

A

shows positions of atoms and every bond

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9
Q

What’s a Structural formula?

A

minimum ordered arrangement of atoms

e.g. CH3CH2CH3

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10
Q

What’s a Molecular formula?

A

shows number and type of atoms

e.g C6H12O6

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11
Q

What’s an Empirical formula?

A

show the smallest whole number ratio of atoms of the elements in a compound

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12
Q

What’s a skeletal formula?

A

simplified formula that uses line and doesn’t show hydrogen’s in alkyl chain

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13
Q

What’s a Structural isomer?

A

molecules with same molecular formula but different structural formulas

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14
Q

What’s a Stereoisomer?

A

molecules with same molecular & structural formula but different arrangements of atoms in space?

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15
Q

What e/z isomerism?

A

type of stereoisomer where different groups arranged around a c double bond

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16
Q

What Cis-Trans isomerism?

A

type of E/Z isomerism but the 2 substituents on each carbons the same

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17
Q

What would an ‘e’ isomer look like?

A

e for enemies

highest priority substituents on opposite ends(diagonal)

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18
Q

What would a ‘Z’ isomer look like?

A

highest priority substituents on the same side of the double bond(straight line)

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19
Q

What would a Cis-isomer look like?

A

same group same side (straight line)

basically z

20
Q

What would a Trans-isomer look like?

A

same groups on opposite sides

basically e

21
Q

What’s Homolytic fission, what’s the product?

A

two covalent bonds break and electrons split equally to creates radicals

22
Q

What’s Heterolytic fission, what’s the product?

A

two covalent bonds break and electrons split unequally

• creates Ions (positive and negative)

23
Q

Summarise Free Radical substitution to form a Haloalkane

A
  1. Initiation- generate radicals with UV light
  2. Propagation- 2 steps
    • radical + alkane→ alkyl radical + acid
    • alkyl radical + halogen → new radical + haloalkane
  3. termination- reactions to remove all remaining radicals
24
Q

What’s an Alkane?

A

Saturated hydrocarbon homologous series

25
What's are some features of Alkanes?
* longer chains = increasing boiling point * only weak London(dispersion) forces * non polar * only σ bonds
26
What happens in Complete combustion?
enough oxygen for substance to burn with clean blue flame and produces max thermal energy + co2 + water
27
What happens in Incomplete combustion?
not enough oxygen for substance to burn. makes orange flame and produces less energy CO2 + water + CO
28
What's an Alkene?
Unsaturated hydrocarbon homologous series
29
What's are some features of Alkanes?
* longer chains = increasing boiling point * can undergo addition reactions * more reactive * contain both π and σ bonds * double bonds so can show sterioisomersm
30
What's a Nucleophile?
electron pair donors | atoms with lone pair electrons & negative ions
31
What's an Electrophile?
electron pair acceptors | positve ions & partial positives
32
How do you go from Alkane to Alkene?
cracking | • High temperatures
33
How do you go from Alkene to Alkane?
Hydrogenation (H2) of Alkenes | • High temperature and nickel catalyst
34
What the difference between halogenation of Alkanes and Alkenes?
``` Alkanes = free radical substitution reaction (needs UV ) alkenes = simple addition reaction ```
35
In Alkene addition mechanisms how do the arrows move
from double bond to electrophile | then nucleophile to carbocation
36
How do you go from an Alkene to an Alcohol?
Hydration with steam(H2O) • High temperature and pressure • Phosphoric acid catalyst
37
How does the type of carbocation affect its stability?
the less hydrogens around the carbocation the more stable | ∴ tertiary carbocation most stable & primary least stable
38
What happens when many Alkenes join together?
forms a polymer
39
What is a Repeating unit?
The structure that repeat over and over again | closed of in brackets with n on outside
40
Why are Polymers useful?
versatile with many uses, are also saturated compounds so they're vey stable
41
Why are landfills a bad way to dispose Polymer waste?
when we bury the rubbish, conditions become anaerobic which reduces the decomposition rate of biodegrable materials
42
Why is combustion a bad way to dispose Polymer waste?(2)
• Polymers release green house gases when burnt(CO2) - Greenhouse gases contribute too climate change • Other plastics may release other toxic gases
43
What are some ways we can combat Polymer waste?
* reduce unnecessary usage * reusing plastics * recycling * using biodegradable polymers * using photodegradable polymers
44
What are Bio & Photo degradable polymer?
* Bio= broken down by microorganisms & the environment | * Photo= breakdown using energy wavelengths similar to light
45
What's a bioplastic?
Material made from renewable source that biodegradable
46
Why is the difference between branched and unbranched hydrocarbons
• Unbranched isomers tend to be longer, ∴ Higher Bp & Mp • Unbranched has more points of contact • Unbranched has stronger/more induced dipole dipole forces
47
uncertainty Eq?
(absolute uncertainty *2)/ value measured