C2 Specimen Flashcards

1
Q

Inital rate of reaction in this experiment has the value 4.57x10-6
Use this value together with a rate obtained from your tangent to justify that the order of reaction is 2 with respect to butandiene

A

Find gradient
Inital rate/gradient = (2.23)

Initial concentration at point where tangent
0.018/0.012 = 1.5

If order 2 rate should increase (1.5)2 = 2.25
Approximately 2.23
So 2nd order with respect butadiene

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2
Q

What would you do if you need to find Mr with two different isotopes (35Cl) and (37Cl)
C8H17Cl

A

C8H17(35Cl) = 148
C8H17(37Cl) = 150
148.8

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3
Q

Explain the origin of the interaction representation by the dotted lines

A

Hydrogen bonding between O- and H+
N and O are both very electronegative
C=O N-H are polar
Lone pair strongly attracted to H+

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4
Q

State the name of the sugar molecule that is attached to the bond at X

A

2-deoxyribose

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5
Q

Suggest which of the bases A and B forms a pair with guanine when messenger RNA is synthesised

A

Base A
Top N-H forms H-bonds to lone pair on O of guanine
Lone pair of electrons on N bonds to H-N of guanine
A lone pair of e- on O bonds to lower H-N

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6
Q

The minimum quantity of hot water was used why

A

To ensure hot solution would be saturated

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7
Q

The crystals were compressed in the funnel why

A

Air passes through sample and not round it

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8
Q

NO2 -> NH2 reagents

A

Sn/HCl

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9
Q

NMR how to describe (decimal integration levels)
IR and NMR

A

IR radiation (O-H) alcohol 3230-3550
Talk about the peaks different H environments
Convert decimal points to whole numbers
Talk about singlet (splitting)

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10
Q

Butanone is reduced in a two step reaction using NaBH4 followed by dilute HCl
Write overall equation for the reduction of butanone using [H] to represent the reducant

A

CH3CH2COCH3 + 2[H] -> CH3CH2CXH(OH)CH3

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11
Q

By considering the mechanism of the reaction, explain whhy the product has no effect on plane polarised light

A

Nucleoophilic attack
Planar carbonyl grouyp
H- attacks from either side

Product of step 1 shown
Two chiral forms
Equal amounts of enatiomer
Optical isomer rotate plane in opposite directions
With racemic mixture

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