Org 1 Flashcards

(34 cards)

1
Q

Aliphatic

A

Straight/branch hydrocarbon

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2
Q

Alicyclic

A

Hydrocarbon ring that is not benzene

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3
Q

Aromatic

A

Contains benzene

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4
Q

Saturated

A

Only single bond between C ( C-C)
Alkanes

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5
Q

Unsaturated

A

At least one double bond (at least one C=C)
Alkenes ( 2 e; double bonds )

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6
Q

Structural isomers

A

Same formula, diff structure

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7
Q

Chain isomers

A

Same formula but branching gives diff properties

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8
Q

Position isomers

A

Same functional group and formula, but functional group in diff. place

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9
Q

Functional group isomers

A

Same formula, diff. functional group

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10
Q

Stereoisomers/ E-Z isomers

A

Same structural formula but diff. arrangement in space
- no free rotation due to C=C

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11
Q

E isomer

A

Non polar

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12
Q

Z isomer

A

Polar

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13
Q

Catalytic cracking

A

Zeolite cat.
450 degrees C
Just above 1atm
More efficient (less E wasted)
Forms branched and cyclic alkanes

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14
Q

Thermal cracking

A

Temp. 400-900 degrees C
Pressure of 700 kPa
Produced many alkenes

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15
Q

Longer alkane chain

A

More London forces

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16
Q

Branched alkane chain

A

Branches reduce changes for dipole interactions

17
Q

Alkene test

A

Decolourises bromine water (electrophilic addition)

18
Q

Alkane from alkene

A

Alkene + H2 in Ni cat. presence

19
Q

Alkene to haloalkane

A

Add hydrogen halid (electro. add.)

20
Q

Alkene to alcohol

A

Steam
Active cat. (Phosphoric)
- OH- added

21
Q

Major reaction product

A

Nucleophile added to C with most bonds to H (more stable)

22
Q

Stability of alkenes from lowest to highest

A

1 primary
2 secondary
3 tertiary

23
Q

During hydrolysis; speed of ppt formation from lowest to highest

A

Primariy
Secondary
Tertiary

24
Q

Haloalkane to alcohol

A

Hydroxide (aq)
Heated under reflux
(Nucl. Sub)

25
Increase haloalkane chain
Potassium cyanide Ammoniy
26
Hydrolysis rate (ppt formation) trend of primary haloalkanes
Halide test Fluoro = unreactive Chloro Bro Iodo = very fast Bond strength increase up the group
27
Potassium dichromate (ox agent) change in primary and secondary alcohols
Orange to green
28
Alcohol to aldehyde (oxidation)
Primary alcohol Potassium dichromate Heat - distillation
29
Aldehyde to carbo. acid (oxidation)
Hey under reflux Potassium dichromate
30
Alcohol to ketone (oxidation)
Secondary alcohols Heat - distillation Potassium dichromate
31
Alcohol to alkene (elimination)
Dehydration (water lost) Conc. H2SO4 or H2PO4 Reflux
32
Alcohol to haloalkane
Add sodium halide Sulfuric acid Heated under reflux
33
Alcohol halogenation
PCl5 or PI3 Or Red phosphorus and iodine
34
Alcohol combustion products
Water and CO2