Organic Chemistry Flashcards

1
Q

What fo primary, secondary and tertiary alcohols oxidise into?

A

Primary: to aldehyde to acid

secondary: to ketone
tertiary: doesn’t oxidise

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2
Q

How to make an ionic equation?

Start with the half equations

A
  1. Remove all the oxygen, and balance with water
  2. Balance the H with H positive
  3. Balance the charge using the electrons
  4. Repeat for the other half equation
  5. Balance both equations and add them to cancel out the electrons
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3
Q

What’s an aldehyde?

A

Chain ENDS with a C connected to a double bond O and a single bond H

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4
Q

What’s a ketone?

A

A carbon not at the end of the chain that is connected to a double bond O

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5
Q

What’s a carbonyl?

A

C bonded to a double bond O and anything. The carbonyl is the CO, but it does not meant that it is not an aldehyde functional group

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6
Q

What’s a carboxylic acid?

A

Carbon chain ends with a C bonded to a double bond O and an OH

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7
Q

How do you oxidise a primary alcohol experimentally?

A

Fractional distillation to oxidise to aldehyde

Distill with reflux to acid- increases the time

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