Organic Revision Flashcards

1
Q

What makes a SN2 reaction?

A

Happens in one step
Nucleophile and electrophile both in rate determining step (Bimolecular)
There is a transition step
Strong nucleophile

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2
Q

What happens to nucleophilicity as you go down the periodic table? Eg, F to Cl, Cl to Br.

A

It increases

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3
Q

What happens to nucleophilicty as you go from left to right of the periodic table? Eg, NH2 to OH, OH to F

A

It decreases

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4
Q

What is steric hindrance?

A

When a nucleophile has big groups which make it harder to fit with the electrophile

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5
Q

Which SN reaction favours tertiary carbons ?

A

SN1

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6
Q

Which SN has a hypothetical transition state?

A

SN2

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7
Q

What SN is bimolecular?

A

SN2

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8
Q

What does unimolecular mean?

A

Only one species is present in the rate determining step

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9
Q

What is the difference between E and SN reactions?

A

E reactions eliminate the leaving group and cause a C=C bond to form.
SN reactions cause a substitute of species, one leaves and another replaces it

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10
Q

What is the Grignard reagent?

A

R-Mg-X

Magnesium bound to a halide and carbon chain

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11
Q

What does sodium borhydiride do?

A

Reduces aldehydes and Ketones

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12
Q

What does LiAlH4 do?

A

It’s a potent reducing agent, reduces most double bond O to alcohols

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13
Q

What is the function of SOCl2?

A

It turns a carboxylic acid into an acid chloride (swaps the OH in COOH for a Cl)

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14
Q

What is the function of potassium dichromate (or other similar reagents which have chromium)?

A

Potent oxidative agents, oxidises alcohols to Ketones and ketones to carboxylic acids

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15
Q

How do you calculate the double bond equivalent?

A

Count the rings and double bonds as 1
Count triple bonds as 2
Add them all up

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16
Q

How do you calculate the pI of an amino acid (isoelectropoint)

A

PKa1+pKa2
——————
2