ORGO 2 lab Final

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Last updated 8:48 PM on 4/23/26
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40 Terms

1
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Please select true below. this question is worth zero points:

True

2
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For esters the C=O stretch occurs at:

1750 - 1730 cm^-1

3
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A good separation on a TLC plate is achieved when each compound:

has a different Rf value

4
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What functional group can be seen in the following IR spectra:

carboxylic acid

<p>carboxylic acid</p>
5
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Rank the following compounds in order of decreasing speed of reactivity in an electrophilic aromatic substitution reaction:

3 > 1 >2

6
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Select the correct mechanism to form a Grignard reagent

7
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Which solvent(s) can be used for a Grignard reaction? select all that apply.

THF

diethyl ether

8
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What way can radical chain growth polymerization terminate?

disproportionation, chain combination or reaction with an impurity

9
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Step-growth polymers have three possible mechanisms; radical polymerization, cationic polymerization, or anionic polymerization

False

10
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A pure solid sample will have a melting point range of approximately of 1 °C or less

True

11
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What is missing from the box shown below

Acid

12
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It is important that the melting point of the solid being recrystallized is above the boiling point of the recrystallization solvent to prevent "oiling out".

True

13
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The best recrystallization solvent dissolves a large amount of your solid at high temperatures, and a small amount of your solid at low temperature

True

14
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Grignard reagents can react with O2 and CO2 to form peroxides and carboxylic acids, respectively

True

15
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In a Fischer esterification reaction, IR analysis can be used to determine whether or not the carboxylic acid has been converted to an ester, because we will see an O-H stretch in the product, but not in the starting material

False

16
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The purpose of adding Na2SO4 to the ester products (from the Fischer esterification reaction) was to remove water

True

17
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The first step of the Fischer esterification mechanism is the protonation of the carbonyl oxygen by an acid catalyst

True

18
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During an electrophilic aromatic substitution reaction, the presence of an electron-donating group on the aromatic ring will _________ the reaction rate

Increase

19
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(Nitration of methyl benzoate reaction)

It is important to add the methyl benzoate to the nitrating solution quickly to prevent the formation of side products.

False

20
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The polymerization of this molecule, goes through three district phases. What are these phases - must be in the correct order

1 Initiation, 2 propagation, 3 termination

21
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The name of this polymer is _________

Nylon 6,8

22
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Using the given reagent bank, select the corresponding number for the missing reagent(s).

21 1,6-hexanediamine

23
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What is the correct temperature for this reaction

0° C

24
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Using the given reagent bank, select the corresponding number for the missing reagent(s).

19 Propanol and H2SO4

25
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What is the correct solvent for this reaction ?

Diethyl ether

26
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Using the given reagent bank, select the corresponding number for the missing reagent(s).

1 HNO3 and H2SO4

27
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Using the given reagent bank, select the corresponding number for the missing reagent(s).

18 Methanol and H2SO4

28
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What is the correct solvent for this reaction ?

0.5 M NaOH

29
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What is the correct temperature for this reaction?

0° C

30
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What is the correct first step in the mechanism for the nitration of methyl benzoate? select all that are correct

31
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What is the correct second step in the reaction?? select all that are correct

32
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Select the main product(s) formed in the nitration of methyl benzoate? select all that are correct.

33
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During the polymer lab, we made Nylon 6,10 from a di-acid chloride and a diamine. This is an example of ___________ polymerization

18. Step-Growth

34
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During an electrophilic aromatic substitution reaction, the rate-determining step involves the aromatic ring attacking a(n)

2. Electrophile

35
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During the polymer lab we made slime from poly(vinyl alcohol) and borax. The strongest force responsible for cross0linking this polymer chains is:

21. Hydrogen-bonding

36
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__________ contain the function group -COOR

25. Esters

37
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is the following spectra methyl propionate, methanol or propionic acid?

methyl propionate

38
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is the following spectra methyl propionate, methanol or propionic acid?

Methanol

39
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is the following spectra methyl propionate, methanol or propionic acid?

propionic acid

40
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Please select true below. this question is worth zero points:

True