Organic synthesis Flashcards

1
Q

What is the general formula for alkanes?

A

C_nH_(2n+2)

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2
Q

True or False: Alkenes are saturated hydrocarbons.

A

False

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3
Q

Fill in the blank: The process of converting an alkene to an alkane is called __________.

A

hydrogenation

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4
Q

What functional group characterizes alcohols?

A

Hydroxyl group (-OH)

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5
Q

Which reaction involves the substitution of a halogen in an alkane?

A

Free radical substitution

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6
Q

True or False: Carboxylic acids can act as both acids and bases.

A

True

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7
Q

What is the primary product when a carboxylic acid reacts with an alcohol?

A

Ester

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8
Q

Name the reaction type that forms an amide from a carboxylic acid.

A

Condensation reaction

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9
Q

What is the main reagent used for the reduction of aldehydes?

A

NABH4 (Sodium borohydride)

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10
Q

Which reagent is commonly used to oxidize primary alcohols to aldehydes?

A

Potassium dichromate (K2Cr2O7)

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11
Q

What is the key feature of a nucleophilic substitution reaction?

A

A nucleophile replaces a leaving group.

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12
Q

True or False: Benzene is a saturated compound.

A

False

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13
Q

What is the mechanism of electrophilic substitution in aromatic compounds?

A

The electrophile replaces a hydrogen atom on the benzene ring.

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14
Q

Fill in the blank: The product of a nitration reaction of benzene is __________.

A

Nitrobenzene

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15
Q

What is the role of sulfuric acid in the synthesis of esters?

A

Catalyst

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16
Q

Which type of reaction is used to form alkenes from alcohols?

A

Dehydration reaction

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17
Q

What is the effect of increasing the chain length on the boiling point of alkanes?

A

The boiling point increases.

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18
Q

True or False: Ethers can be hydrolyzed to form alcohols.

A

True

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19
Q

What is the primary use of thin-layer chromatography (TLC) in organic analysis?

A

To separate and identify compounds.

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20
Q

What does the retention factor (Rf) indicate in chromatography?

A

The distance traveled by the compound relative to the solvent front.

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21
Q

Fill in the blank: The process of breaking down a compound into simpler substances is called __________.

A

decomposition

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22
Q

What type of reaction occurs when an alkene reacts with a halogen?

A

Electrophilic addition

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23
Q

Name one method of preparing alkenes from alkanes.

A

Cracking

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24
Q

True or False: Primary alcohols can be oxidized to carboxylic acids.

A

True

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25
Q

What is the main product of the hydrolysis of esters?

A

Carboxylic acid and alcohol

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26
Q

What is the significance of using a reflux apparatus in organic synthesis?

A

To heat a reaction mixture without losing volatile components.

27
Q

Which spectroscopy technique is used to determine the structure of organic compounds by measuring the vibrations of bonds?

A

Infrared spectroscopy (IR)

28
Q

Fill in the blank: The process of heating a compound with a strong acid to break it down is called __________.

A

acid hydrolysis

29
Q

What type of isomerism is exhibited by alkenes?

A

Geometric (cis-trans) isomerism

30
Q

True or False: All alcohols can form hydrogen bonds.

31
Q

What is the role of a drying agent in organic synthesis?

A

To remove water from organic solvents.

32
Q

Name the type of reaction where two molecules combine to form a larger molecule with the loss of a small molecule.

A

Condensation reaction

33
Q

What is the common name for ethanoic acid?

A

Acetic acid

34
Q

Fill in the blank: The reaction of an acid and a base to form a salt and water is called __________.

A

neutralization

35
Q

What type of chemical reaction occurs when a compound loses electrons?

36
Q

What is the main characteristic of a primary amine?

A

One alkyl group attached to the nitrogen atom.

37
Q

True or False: Aromatic compounds are more reactive than aliphatic compounds.

38
Q

What is the purpose of recrystallization in organic chemistry?

A

To purify solid compounds.

39
Q

What is needed to turn nitrobenzene into phenylamine?

A

Reduction using Sn and concentrated HCl.

40
Q

How do you convert ethene into ethanoic acid?

A

Add H2SO4 with water and reflux with acidified potassium dichromate.

41
Q

What reagents are needed to convert benzene into 1-phenylpropanone?

A

Friedel-Crafts acylation using propanoyl chloride and AlCl3.

42
Q

What must be thoroughly investigated before commercial production of a compound?

A

Effectiveness, safety, side effects, and so on.

43
Q

What is the first step in working out a synthesis scheme?

A

Write down the formula of the starting molecule (A) and the target molecule (X).

44
Q

List the functional groups you should know for organic synthesis.

A
  • Alkanes
  • Alkenes
  • Halogenoalkanes
  • Alcohols
  • Amines
  • Aldehydes
  • Ketones
  • Acid derivatives
  • Arenes
45
Q

What does ‘yield’ measure in organic synthesis?

A

The efficiency of the conversion of a starting material into a product.

46
Q

Why is it important to keep the number of steps in a synthesis scheme small?

A

To maximise the yield of the target.

47
Q

Fill in the blank: The reaction of cyanide ions with a __________ will be needed if the target molecule has one more carbon atom than the starting material.

A

halogenoalkane

48
Q

How do you convert propanone into 2-bromopropane?

A

Reduce with NaBH4 to to propan-2-ol and then react with KBr/H2SO4

49
Q

What potential does the target compound have after synthesis?

A

Potential for use in reactions and processes.

50
Q

What is the significance of atom economy in organic synthesis?

A

It relates to the efficiency of the conversion process.

51
Q

How do you convert cyclohexanol into cyclohexene?

A

Dehydrate with P2O5

52
Q

How do you turn but-1-ene into butanone?

A

Conc. sulphuric acid with water and then oxidise with acidified potassium dichromate

53
Q

What do you need to turn ethanoic acid into methyl ethanoate?

A

Methanol with an acid catalyst

54
Q

What reagent do you need to make but-1-ene into butan-2-ol?

A

Conc. sulphuric acid with water

55
Q

What should you react 1-bromobutane with to get pentanenitrile?

A

Potassium cyanide

56
Q

What is the role of hydrogen and nickel in turning a nitrile into an amine?

A

Hydrogen reduces the nitrile and nickel acts as a catalyst

57
Q

Fill in the blank: Secondary alcohols are oxidised to _______.

A

ketones

This is part of the oxidation process in organic chemistry.

58
Q

What oxidising agent is used to oxidise primary alcohols to aldehydes?

A

Potassium dichromate (VI)

It is acidified with dilute sulfuric acid for this reaction.

59
Q

What is the outcome of oxidising aldehydes?

A

Carboxylic acids

Aldehydes can be further oxidised to form carboxylic acids.

60
Q

What should you be able to recall regarding functional groups?

A

Reactions and conditions such as heating, refluxing, acidic or alkaline conditions, and catalysts

Understanding these aspects is crucial for organic synthesis.

61
Q

True or False: Propylamine can be made from ethene.

A

True

Ethene can be made into a haloalkane and then reacted with KCN

62
Q

What is the significance of the inter-relationships between functional groups?

A

They help in revising knowledge of organic reactions

Understanding these relationships is key to successful synthesis.

63
Q

What is a common method to produce a library of aldehydes from alcohols?

A

Oxidising several alcohols of different chain lengths

This method allows for the exploration of various compounds’ medicinal potential.

64
Q

Fill in the blank: The reaction of cyanide is an example of a reaction that may involve _______.

A

functional groups

This highlights the importance of functional groups in synthetic reactions.