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Chemistry Unit #5: Organic Chemistry Topics Test on Friday, February 10, 2017

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

Test

Back (Answer)

…………………………………….O Cr₂O₇²⁻/H⁺………………….|| Primary alcohol ===> CH₃ - CH₂ - CH₂ - OH =========> CH₃ - CH₂ - CH ………………………………………………………………………………………………(aldehyde)

#2
Front (Question)

Compare and contrast catalytic cracking to catalytic reforming.

Back (Answer)

Similarities They both need catalysts Used to make fuels Oxygen cannot be present Differences Catalytic cracking makes smaller chains from larger ones while catalytic reforming produces longer chains from smaller ones

#3
Front (Question)

What does orange turn into when Alcohol is warmed with Cr₂O₇²⁻/H⁺ (acidified potassium dichromate)? It is the basis behind the breathalyser test.

Back (Answer)

Orange will turn to green

#4
Front (Question)

What is the name and reduced formula of this structural formula? CH₃ — CH₂ — CH₂ — CH₃

Back (Answer)

C₄H₁₀ and butane

#5
Front (Question)

What is the Catalyst for the Oxidation of Alcohols?

Back (Answer)

Cr₂O₇²⁻/H⁺ (acidified potassium dichromate)

#6
Front (Question)

What forms from the Oxidation of Primary Alcohols?

Back (Answer)

Aldehydes

#7
Front (Question)

What chemical process may be used to convert the petroleum distillation residue into gasoline?

Back (Answer)

Catalytic cracking

#8
Front (Question)

What are the 4 Alkene Addition Reaction

Back (Answer)

1.) Halogens: (F₂, Cl₂, Br₂, I₂) CH₃ — CH = CH₂ + Br₂ ===> CH₃ — CHBr — CH₂Br 2.) Hydrogen gas, H₂ (Turns it into alkane) CH₂ = CH₂ + H₂ ===> CH₃ — CH₃ 3.) Water, H₂O (Makes an alcohol) CH₃ — CH = CH₂ + HOH ===> CH₃ — CH₂ — CH₂OH 4.) Hydrogen halides; (HF, GCl, HBr, HI) CH₃ — CH = CH — CH₃ + HBr ===> CH₃ - CHBr — CH₂— CH₃

#9
Front (Question)

What forms from the Oxidation of Secondary Alcohols?

Back (Answer)

Ketones

#10
Front (Question)

What is the name and reduced formula of this structural formula? CH₃ — CH₂ — CH₂ — CH₂ — CH₂ — CH₃

Back (Answer)

C₆H₁₄ and hexane

#11
Front (Question)

How does the average number of carbon atoms per molecule vary for the fractionation product location shown in figure H2. Explain this order using IMF. (2)

Back (Answer)

As the number of carbons on the chains increase, they are distilled lower in the tower. This occurs because the longer chains have more IMF, resulting in higher boiling points

#12
Front (Question)

What forms from the Oxidation of Tertiary Alcohols?

Back (Answer)

Tertiary Alcohols cannot undergo this reaction

#13
Front (Question)

What is the product of this Nucleophilic Substitution of Halogenalkanes? CH₃ | CH₃ - C - CH₃ + OH⁻ ===> | Cl

Back (Answer)

CH₃ | CH₃ - C - CH₃ + Cl⁻ | OH

#14
Front (Question)

What is the name and reduced formula of this structural formula? CH₃ — CH₂ — CH₂ — CH₂ — CH₃

Back (Answer)

C₅H₁₂ and pentane

#15
Front (Question)

What physical property is used to separate different compounds in a petroleum fractionation tower?

Back (Answer)

Boiling point

#16
Front (Question)

What is the name and reduced formula of this structural formula? CH₃ — CH₂ — CH₂ — CH₂ — CH₂ — CH₂ — CH₃

Back (Answer)

C₇H₁₆ and heptane

#17
Front (Question)

What is the name and reduced formula of this structural formula? CH₂ — CH₂

Back (Answer)

C₂H₆ and ethane

#18
Front (Question)

What is the name and reduced formula of this structural formula? CH₃

Back (Answer)

CH₄ and methane

#19
Front (Question)

What is the name and reduced formula of this structural formula? CH₃ — CH₂ — CH₂ — CH₂ — CH₂ — CH₂ — CH₂ — CH₃

Back (Answer)

C₈H₁₈ and octane

#20
Front (Question)

What is the name and reduced formula of this structural formula? CH₃ — CH₂ — CH₃

Back (Answer)

C₃H₈ and propane

#21
Front (Question)

What is the name of this structure? CH₃ CH₂ — CH₂ — CH₃ | | CH₃ = C — CH — CH — CH₂ — CH₂ — CH₃ | CH₂ — CH₃

Back (Answer)

3-ethyl-2-methyl-4-propyl-1-heptene

#22
Front (Question)

What are the three factors on which Boling point depends on? 3 + (3 - 4 explanations)

Back (Answer)

Polarity Substances with hydrogen bonding have higher boiling points than those with dipole-dipole or only London Dispersion. Alkanes, alkenes, and benzne are non-polar with only London Dispersion forces Aldehydes, ketones, and esters experience the stronger dipole-dipole forces Amines, alcohols and carboxylic acids exhibit hydrogen bonding (highest Boling Point) Molar Mass Generally, higher molar mass means higher boiling points for non-polar molecules CH₄ gas at room temperature Liquid at room temperature Very long chains form waxy solids Straight vs. Branched chains Straight chains have higher boiling point Branching makes molecules more spherical, reducing contact surface area Less attraction between molecules

#23
Front (Question)

What are the 3 main points on Benzene?

Back (Answer)

Benzene does not undergo addition reaction, but rather substitution reactions, Benzene does not react with KMnO₄, Benzene’s carbon bonds are equivalent, Therefore benzene cannot have double bonds.

#24
Front (Question)

What is the Polymerization of this? CH₂ = CHCl ==============>

Back (Answer)

(Polymerization) CH₂ = CHCl ==============> — CH₂ — CHCl —