Exam 1 Flashcards

1
Q

Definition of Polymers

A

Large macromolecules which are made of many repeating units of smaller molecules.

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2
Q

Types of polymers

A
  • Addition polymers
  • Condensation polymers
  • Polyamides
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3
Q

Definition of Addition polymers

A

monomers’ double bonds are broken and the molecules form a long chain

Ex- polyethylene, polyvinyl chloride, polystyrene.

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4
Q

Def of Condensation polymers

A

Bifunctional monomers react to form a long-chain polymeric molecule

Ex- Nylons, polyesters, polysaccharides.

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5
Q

def of Polyamides

A

formed when compounds with a COOH functional group react with NH2 group.

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6
Q

What does the number after nylon mean?

A

The number of carbon atoms present in each of the original reactants.

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7
Q

What technique was used to prepare Nylon in the lab?

A

Interfacial Polymerization (reaction occurs at the interface of two solutions)

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8
Q

Why was sebacoyl chloride used instead of carboxylic acid in the nylon reaction?

A

Acid chlorides are much more reactive than acids are

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9
Q

Why is NaOH used in the Nylon Reaction?

A

It is used to neutralize the HCl byproduct of the reaction

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10
Q

Why are plasticizers added to polymers?

A

They help to improve the flexibility and extensibility of the polymer

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11
Q

Chemiluminescence Definition

A

The emission of light as the result of a chemical reaction

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12
Q

What is the name of the chemical responsible for firefly light?

A

Luciferase

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13
Q

What is the chemical responsible for producing light in a glow stick?

A

Luminol and Oxalate reactions

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14
Q

Practical uses of compounds with chemiluminescent properties

A
  • Forensic science
  • Spectroscopy
  • Medical diagnosis
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15
Q

Diene Definition

A

unsaturated hydrocarbon containing two double bonds. Must be conjugated and in s-cis- conformation.

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16
Q

Dienophile Def

A

An alkene or Alkyne that readily reacts with a diene.

17
Q

Adduct Def

A

The product of the diels alder reaction incorporating the reactants

18
Q

What is the thermometer reading during the collection of cyclopentadiene?

A

41 C

19
Q

Why is cyclopentadiene prepared right before using it?

A

If stored at room temperature, it is completely converted into the dimer.

20
Q

How was cyclopentadiene added to the solution of Maleic anhydride?

A

It was added using a dropper while the anhydride was in an ice bath

21
Q

Why was Cyclopentadiene added slowly to maleic anhydride?

A

The reaction is exothermic and overheating with splashing will occur if the cyclopentadienyl is added too fast.

22
Q

Why was a mixture of solvents used in the DA rxn?

A

To maintain thermal equilibrium so the adduct will form

23
Q

Why is the nitration of methyl benzoate performed at a low temp?

A

Temp must be kept below 15 C to prevent the formation of byproducts.

24
Q

How was the filtrate neutralized?

A

The filtrate is poured into 30 ml of water and 8g of Sodium carbonate is added

25
Q

The main product of nitration of methyl Benzoate

A

The reaction is regioselective, Methyl 3-nitrobenzoate

26
Q

What are some possible side products of Nitration if the temp is not kept low?

A

The methyl 3,5 Dinitrobenzoate product

27
Q

Why is the yield of the nitration reaction low?

A

multiple vacuum filtrations