organic analysis Flashcards
to identify whether our substance contains an alkene functional group we use
bromine solution
we put a sample of our test in a test tube
and add a few drops of bromine solution
bromine solution is brownish reddish
it changes from brownish to colourless if C=C are present (alkenes functional group)
We can test whether we have a tertiary alcohol using
H+ / K2Cr2O7 (acidified potassium dichromate)
if we add it to our sample and our solution remains orange we have tertiary
if it changes to green we have a primary and secondary alcohol present
what is the test identify primary or secondary alcohol
we add tollens reagent
if we have a primary = aldehyde it turns into a silver mirror
if it’s colourless it’s secondary alcohol =ketone
name the reagent you could add to a solution to test for the presence of ethanolic acid
carbonate or magnesium
name a reagent you could add to a solution to test for presence of ethene
Name the reagent you could add to a solution to test for the presence of 2-ethylhexan-2-ol or 2-ethylhexan-1-ol
acidified potassium dichromate
Acidified potassium dichromate is added to a solution containing either propan-1-ol or propan-2-ol.
Name a reagent you could add to the resulting solution to test if the original alcohol is propan-1-ol or propan-2-ol.
tollens reagent / benedict’s solution
name a reagent you could add to a solution to test for the presence of hex-3-ene
bromine solution
name a reagent you could add to a solution to test for the presence of formaldehyde
tollens reagent
Name a reagent you could add to a solution to test for the presence of 3-methylpentanoic acid
carbonate or magnesium
chemist has discovered that the labels have fallen off four bottles each of which contains a different organic liquid. These liquids are known to be butanal, butanoic acid, butan-1-ol and 1-bromobutane.
Suggest a series of 3 test-tube reactions which could be used to determine which compound is in which bottle.
For each test, state the reagents used and the observations expected.
[6 marks]
If the solution is a primary alcohol we add tollens reagent to find that which will turn it into a silver precipitate which indicates it’s butanal
if there’s no colour present it’s another molecule. We then add acidified potassium dichromate, if there’s a secondary or primary alcohol present it will turn green so it’s butan-1-ol but if it’s colourless it’s another molecule.
we then add sodium carbonate to the solution. if its giving bubbles then it’s a carboxylic group ( butanoic acid) if not it’s 1-bromobutane
What would you add to a solution to distinguish between propan-2-ol and methylpropan-2-ol
what would happen if we add this to propan-2-ol and 2-methylpropan-2-ol?
acidified / H+
potassium dichromate
if we add it to propan-2-ol it will turn green
if we add it to 2-methylpropan-2-ol there’s no change it will remain orange
Calculate the masses of propanone and butanone to 5 decimal places, using the relative isotopic mass data below. You can assume that no other isotopes are present
Hydrogen-1: 1.00783
Carbon-12: 12.00000
Oxygen-16: 15.99491
Propanone= (3x 12.00000) + (6x 1.00783) + (1x 15.99491) = 58.04189
butane = (4x 12.00000) + (10x 1.00783) = 58.07830
What is the general formula of methyl propane’s
C4H10
What is fragmentation
when molecular ions split into 2 or more parts called fragments
fragmentation is especially likely when the ionisation method is
electron impact as it makes fragmentation occur more likely
What do these lines tell us about
the molecules structure
What are the fragments to look for for this molecule?
it can divide into 3
CH3+ = m/z 15
C2H5+ = m/z 29
C3H7+ = m/z 43
Explain what the method is for chromatography
1) start with piece of glass, plastic or metal coat it with a thin layer or silica (SiO2) or aluminia (Al2O3) which is called coated sheet
2) draw a pencil line near the bottom of the plate and add a small drop of a sample then place a plate into the beaker containing a solvent. There should be enough to cover bottom of there coated sheet but it shouldn’t touch the line
4) then cover the solvent and wait for it to rise the coating then is soaked by the solvent causing it to rise and seperate into 3 dots whilst it rises
What’s the solvent that moves the component called?
moving phase
what’s the thing that moves through the coated sheet
stationary phase
Ethanol could form hydrogen bonds to the stationary phase (silica gel)
Therefore, ethanol adsorbs strongly to the stationary phase.
As a result, retention of ethanol by the stationary phase is
high
because hydrogen bonds can form between them
the distance a component moves can be partly explained by
by the level of retention of the component by the stationary phase and whether the component and the stationary phase are both polar or could form hydrogen bonds
Retention will be high if
both component and stationary phase are polar or if hydrogen bonds can form between them