Elements Of Life Flashcards
Nucleus of the atom?
Most of the mass of the atom is concentrated in the nucleus.
The diameter of the nucleus is smaller compared to the whole atom.
The nucleus is where all the neutrons and protons are found.
Masses + Charge Of Protons, Neutrons + Electrons?
Proton - 1 (Mass), +1 (Charge),
Neutron - 1 (Mass), 0 (Charge),
Electron - 1/2000 (Mass), -1 (Charge).
Nuclear symbols?
This is basically what’s on the periodic table.
(But on a chemistry exam question, it may give you an example of a nuclear symbol and your expected to write it the same way as them).
- Mass number,
- Atomic number,
- Element number.
Neutral, negative and positive atoms?
For neutral atoms, which have no overall charge, the amount of protons should be the same as the electrons.
Negative ions have more electrons than protons.
Positive ions have more protons than electrons.
E.g. Mg2+ is a positive ion because it has lost 2 electrons and therefore has 2 more protons than electrons.
How has the current model of the atom developed?
- Ancient Greeks through that all matter was made from invisible particles.
- At the start of the 19th century, John Dalton described atoms as solid spheres, and said that different spheres made up different elements.
- Scientists did more experiments and our current model began to emerge our current model.
In 1897, J J Thomson did a series of experiments that concluded that atoms weren’t solid and invisible.
- He measured the charge and made and showed that an atom must contain smaller, negatively charged particles (electrons). He called electrons ‘corpuscles’.
- The idea of atoms being solid spheres. The new model was known as the ‘plum pudding model’ - positively charged sphere with negative electrons embedded everywhere in it.
How was the plum pudding model proved to be wrong?
Ernest Rutherford and students - Hans Geiger and Ernest Marsden - 1909.
Conducted Geiger-Marsden experiment. They fired alpha particles (positively charged) at an extremely thin sheet of gold. It was expected that most of the particles would be deflected very slightly by the positive ‘pudding’ that made up most of the atom.
What actually happened? Most of the alpha particles passed straight through the gold atoms, and a very small number were deflected backward (more than 90 degrees).
This showed the plum pudding model couldn’t be right.
So Rutherford came up with a model that could explain this new evidence- the nuclear model of the atom.
Rutherfords model (the nuclear model) stated there is one positively charged nucleus and a cloud of freely orbiting negative electrons surrounded by empty space.
How was Rutherfords nuclear model proved wrong?
Henry Moseley discovered that the charge of the nucleus increased from one element to another in units of one.
This led Rutherford to investigate the nucleus further he discovered protons in the nucleus. The charges of the nuclei of different atoms could then be explained - atoms of different elements have different number of protons.
There was still one problem with the model - the nuclei of atoms were heavier than they would be if they just contained protons - this lead to the discovery of neutrons by James Chadwick.
The Bohr model?
Scientists realised that if the electrons were in a ‘cloud’, then they would spiral down into the nucleus, causing the atom to collapse.
Niels Bohr proposed a new model of the atom with four basic principles:
- Electrons can only exist in fixed orbits, or shells,
- Each shell has a fixed energy,
- When an electron moves between shells, electromagnetic radiation,
- Because the energy of shields is fixed, the radiation will have a fixed frequency.
The frequencies of radiation emitted and absorbed by atoms were already known from experiments. The Bohr model fitted these observations.
The Bohr model also explained why some elements (noble gases) are inert. It said that the shells of an atom can only hold fixed numbers of electrons, and that elements reactivity is due to electrons.
When an atom has full shells of electrons, it is stable and does not react.
What model of atomic structure do we use today?
The Bohr model is widely used to describe atoms because it’s simple and explains may experiments, like bonding and ionisation energy trends.
The most accurate model we have today involves complicated quantum mechanics. Basically, we never know what direction an electron is going in or where it is. But, we can say how likely it is to be at a particular point.
Electrons can act as waves as well as particles.
This model might be more accurate, but it’s harder to get your head around and visualise. It does explain some observations that can’t be accounted for by the Bohr model. We use whatever model is most useful.
Difference between empirical and molecular formula?
Empirical formula - gives the smallest whole number ratio of a time in a compound.
Molecular formula - gives to actual number of atom (ratio) in a molecule.
E.g. a molecule has the empirical formula C4H3O2. It’s molecular mass is 166. What is the molecular formula?
1. Work out Mr. Mr C4H3O2 = 83.
2. Molecular mass (so mass of atoms actually used in reaction) is 166. So do 166/83 = 2
3. Times everything in empirical formula by 2.
C8H6O4.
Relative Atomic Mass?
Ar.
The average relative isotopic mass of naturally occurring isotopes of an element, whilst taking into account their abundances. Masses of atoms are compared to Carbon-12.
Not usually a whole number because it is an average.
E.g. 35Cl and 37Cl - isotopic masses are 35 and 37. Relative atomic mass is 35.5.
Ar values have no units.
Calculation Ar?
Working out Ar:
You can do this normally by adding all the relative atomic mass values of the atoms. E.g. H2O = (1x2) + 16 = 18.
You can also do this using a mass spectrum diagram.
Times all the peak numbers (relative abundance) by the x-axis number that they align with. Then add them all.
Then divide this number by the total sum of all the peaks (which should be the total relative abundance).
Then times this all by 100.
Relative Masses Can Be Measured Using?
Using a mass spectrometer.
Mass spectrometers can tell you: relative atomic mass, relative molecular mass, relative isotopic abundance, molecular structure, and your horoscope.
How Does A Mass Spectrometer Work?
Steps Of How It Works:
1. Vaporisation - the sample is turned into a gas (vaporised) using an electrical heater.
- Ionisation - the gas particles are bombarded with high-energy electrons to ionise them. Electrons are knocked off the particles, leaving positive ions.
- Acceleration - the positive ions are accelerated by an electrical field.
- Detection - the time taken for the positive ions to reach the detector is measured. This depends on an ions mass and charge - light, highly charged ions will reach the detector first, whilst heavier ions with a smaller charge will take longer. For each sample analysed, a mass spectrum is produced.
How To Read A Mass Spectrum?
Y-axis - gives the abundance of ions, often as a percentage. For an element, the height of each peak gives the relative isotopic abundance. E.g. 35Cl has abundance of 75.5%.
If the sample is an element, each line on the graph will represent a different isotope of the element.
The X-axis units are given as a mass/charge ratio. Since the charge of ions is mostly +1, you can often assume the x-axis as simply the relative mass.
How Can Ar Be Worked Out From Mass Spectrum?
If relative abundance is given as a percentage:
1. For each peak, read the % relative isotopic abundance from the y-axis and the relative isotopic mass from the x-axis. Multiply these numbers together for each isotope.
- Add up these totals.
- Divide the total by 100 (because percentages were used).
If relative abundance is not given as a percentage:
1. For each peak, read the % relative isotopic abundance from the y-axis and the relative isotopic mass from the x-axis. Multiply these numbers together for each isotope.
- Add up these totals.
- Then, add up all of the relative abundance’s (the peak numbers) and add them together. Divide the total from step 1 by this number.
- (You can also work out relative isotopic abundance by timesing this number by 100 and giving the answer as a percentage).
Ions?
Ions have different numbers of protons and electrons (this number is usually the same).
Negative Ions - have more electrons than protons.
Positive Ions - have fewer electrons than protons.
Molar Mass?
The same as relative molecular mass.
How to balance equations?
Same number of atoms on both sides.
Equations can also use 1/2 to make some equations balance.
What Are Isotopes?
Atoms of the same element.
They have the same atomic number (number of protons - bottom number on periodic table).
They have different mass numbers (number of neutrons - top number on periodic table).
E.g. chlorine: Cl with 17 protons and 18 neutrons. Isotope of Cl with 17 protons and 20 neutrons.
Relative Isotopic Mass?
Always a whole number. Relative isotopic mass is the mass of an atom of an isotope on a scale where an atom of Carbon-12 is 12.
E.g. 35Cl and 37Cl - isotopic masses are 35 and 37. Relative atomic mass is 35.5.
Ionic equations?
Ionic equations only show the reacting ions in the reaction and the products that the reacting products form.
Ionic equations can only involve ions in solutions. So we don’t break down H2O into H+ and O- because H2O doesn’t dissolve in solutions.
- Balance the equation.
- Break up the equation into ions. E.g. HNO3 would split into H+ and NO3- (remember that H is always positive). We don’t break down anything that doesn’t dissolve in a solution, e.g. H2O.
- Cancel the ions that are repeated on both left and right side of the equations.
Once an ionic equation has been established, check the charges are balanced, as well as the atoms.
If the charges don’t balance, the equation is wrong.
E.g. ionic equation: H+ + OH- —> H2O
Net charge on left = +1 from H and -1 from OH so the net charge is 0. The net charge on the right side is also 0.
Number Of Moles Equation?
Moles = Number Of Particles You Have / Avogadro’s Constant
How Is Mol Calculated In Concentration?
Unit: mol dm-3.
Number Moles = Concentration x Volume (dm3)
If the volume is given in cm3, then we need to divide the volume by 100. This will give the units in dm3.
A hydrocarbon is burnt in excess oxygen. 4.4g or carbon dioxide and 1.8g of water is made. What is the empirical formula of the hydrocarbon?
A hydrocarbon has a H and an C.
We use n = mass/Mr.
H2O: 1.8/18 = 0.1
CO2: 4.4/44 = 0.1
Now, because there is 2 hydrogen atoms in H2O, we know that the original compound from which is was created should have 0.2 moles of hydrogen atoms (0.1 x 2).
Because there is 1 carbon atom in CO2, we know that the hydrocarbon must has 0.1 moles of carbon atoms (0.1 x 1).
This creates a ratio. C:H = 0.1 : 0.2.
This tells us the empirical formula should be CH2.
Relative Molecular Mass?
Also known as relative formula mass and molar mass.
Average mass of a molecule or formula unit on a scale where carbon-12 is 12.
E.g. C2H6O - (2x12) + (6x1) + 16 = 46
This also means that one mole of C2H6O weights 46g.
Aluminium reacts with oxygen to form aluminium oxide, Al2O3. Calculate the number of grams of Al2O3 that could be produced if 2.5g of aluminium and 2.5g of oxygen were allowed to react?
Write balanced equation.
4Al + O2 —> 2Al2O
M/Mr = n.
- 5 / (Al Mr) = 0.09 n
- 5 / (O Mr) = 0.07 n
Al2O Mr = 102
Use equation to find ratios.
4Al = 2Al2O
0.09 = 0.045. 0.045 x 102 = 4.59g of Al2O.
The ratio of moles of oxygen to Al2O is 3:2.
- 07/3 = 0.02. 0.02 x 2 = 0.046.
- 046 x 102 = 4.76g
This means that Al is the limiting reactant because it produces less grams of Al2O than O.
The amount of grams of Al2O that can be made is 4.59g because the reaction is limited by Al.
A compound has a percentage composition of 56.5% potassium, 8.7% carbon and 34.8% oxygen by mass. Calculate the empirical formula?
So imagine the percentages are grams.
K: 56.5/39.1 (mr) = 1.45 moles.
C: 8.7/ 12 = 0.725
O: 34.8/16 = 2.18
Divide each by the smallest.
K: 1.45/0.725 = 2
C: 0.725/0.725 = 1
O: 2.18/0.725 = 3
So the ratio is 2:1:3
Empirical formula: K2CO3
What is water of crystallisation?
Water molecules that are incorporated into another compound.
Hydrated compounds contain them and anhydrous compounds don’t.
One mole of a hydrated compound always contains the same Humber of moles of water of crystallisation (always a whole number too).
E.g. hydrated iron (III) chloride has six moles of water for every mole of iron chloride. So the formula is FeCl3 •6H2O
You beat a hydrous compound to make it anhydrous. If you know the mass of a compound before and after heating, you can work out it’s formula.
4.6g of alcohol, with molar mass 46g, is burnt in excess oxygen. It produces 8.8g of carbon dioxide and 5.4g of water. Calculate the empirical formula?
H2O: 5.4/18 (mr) = 0.3 moles
CO2: 8.8/44 = 0.2 moles
We can always find the amount of carbon and hydrogen atoms from the products.
There is 1 carbon atom in CO2 , so we know that there must be 0.2 moles of C in the original compound.
There is 2 hydrogen atoms in H2O, so we know that there must be 0.6 moles of hydrogen moles in the original comping (0.3 x 2).
We then need to work out the oxygen.
There’s 4.6g of the compound all together, so we do:
0.6 x 1 (H) = 0.6g
0.2 x 12 (C) = 2.4g
4.6 - 0.6 - 2.4 = 1.6g (this is the grams of oxygen).
So then, 1.6/16 (mr) = 0.1 moles
This can then be put as a ratio of C:H:O = 2:6:1
This is empirical formula: C2H6O
Heating 3.210g of hydrated MgSO4•XH2O forms 1.567g of anhydrous magnesium sulfate. Find the value of X and write the formula of the hydrated salt.
(You did this by yourself first time).
- 210 - 1.567 = 1.643g (mass of water lost through heating).
- 643 / 18 (mr) = 0.09
- 567 / 120.4 (mr of MgSO4) = 0.013 (we use this mass and not the 3.210 because we’re finding the mass without the water in).
Divide both by smallest.
- 09/0.013 = 7
- 013 / 0.013 = 1
Ratio is 7:1
MgSO4•7H20
X = 7
Percentage yield equation?
Actual yield / theoretical yield x100%
Theoretical yield = mass of product that should be made in the reaction if no chemicals are lost in the process.
Actual yield = the actual mass of the product (always less). Reasons for this are: sometimes chemicals don’t fully react and some chemicals are lost (e.g. left on filter paper).
Ethanol can be oxidised to form ethanal: C2H5OH + (O) —> CH3CHO + H2O. 9.2g of ethanol was reached with an excess of oxidising agent and 2.1g of ethanal was produced. Calculate the percentage yield?
(You did this first time).
(O) just means an oxidising agent.
We know from the question that the actual yield is 2.1g cause that is what has been produced.
We need to work out theoretical yield.
9.2g of C2H5OH.
M / mr = n
9.2g / 46 = 0.2 moles
0.2 x 44 (mr of CH3CHO) = 8.8g so this is theoretical yield.
Use equation.
Percentage yield = actual /theoretical x100%
2.1 / 8.8 x100 = 24%
What is a standard solution?
Any solution that you know the concentration of.
How to make one:
E.g. make 250cm3 of a 6.00mol dm-3 solution of sodium chloride.
- Work out how many moles of solute you need. Moles = concentration x volume (/1000 to find dm3)
= 6.00 x 250 = 1.5mol - Now work out how many grams of solute is needed.
Mass = moles x Mr = 1.5 x 58.5 (mr of sodium chloride).
(Practical bit)
Place beaker on scales and zero scales.
Weigh out this mass of solute.
Add distilled water to beaker until the solute has dissolved.
Tip solution into volumetric flask (should be an appropriate size). Use a funnel to make sure it all goes in.
Rinse the beaker and rod with distilled water and add that to the flask too. This makes sure there’s no solute clinging to beaker or rod.
Now top the flask up with the correct volume (250cm3) with more distilled water. Make sure bottom of the meniscus reaches the line - use a pipette the closer to the line you get).
Use a stopper on the bottle and mix it.
Check the meniscus again.
When making a standard solution, always make sure it s a suitable concentration compared to the solution your titrating it against. If it’s too dilute, you’ll have to add loads but if it’s too concentrated, the results can be inaccurate easy. A good rule: it should be a similar concentration to the solution it’s being titrated against.
Flame Tests?
Flame test is a test to detect metal ions.
Compounds of some metals give a characteristic colour when heated. This is the idea behind flame test. Here is how to do a flame test:
1) Dip a nichrome wire loop in concentrated hydraulic acid.
2) Then dip the wire loop into the same sample of the compound.
3) Hold the loop in the clear blue part of the Bunsen flame.
4) Observe the colour change in the flame.
You can use these colour changes to detect and identify different ions.
Flame Test Result For Lithium?
Lithium (Li+) turns a crimson colour.
Flame Test Result For Sodium?
Sodium (Na+) turns a orange-yellow colour.
Flame Test Result For Potassium?
Potassium (K+) turns a lilac.
Flame Test Result For Calcium?
Calcium (Ca2+) turns a brick red.
Flame Test Result For Barium?
Barium (Ba2+) turns a green.
Flame Test Result For Copper?
Copper (Cu2+) turns a blue-green.
Test For Hydroxide Metal Ions?
Many metal hydroxides are insoluble and precipitate out of solution when formed. Some of these hydroxides have a characteristic colour. So in this test you:
1) Add a few drops of sodium hydroxide solution to a solution of your mystery compound in the hope of forming an insoluble hydroxide.
2) If you get a coloured insoluble hydroxide, you can then identify the metal ion that was in the compound.
NaOH isn’t the only solution that can be used for precipitation reactions - you can use other hydroxide solutions too.
Identify Metal Ion From A Coloured Insoluble Hydroxide?
Silver (Ag+) - brown (precipitate of silver oxide),
Calcium (Ca2+) - white,
Lead (||) (Pb2+) - white,
Copper (Cu2+) - blue,
Iron (||) (Fe2+) - green,
Iron (|||) (Fe3+) - reddish brown,
Zinc (Zn2+) - white at first, redissolved in excess NaOH to form colourless solution,
Aluminium (Al3+) - white at first, redissolved I’m excess NaOH to form a colourless solution.
Testing For Carbonates Using Hydrochloric Acid?
Hydrochloric acid can help detect carbonates.
This is a test for carbonate ions (negative ions).
1) Take dilute Hydrochloric acid. Carbonates (CO3,2-) will fizz in hydraulic acid to give off carbon dioxide.
2) Capture the gas given off.
3) Test for carbon dioxide using lime water.
Carbon dioxide turns lime water cloudy. To do this: bubble the gas through a test tube of lime water and watch what happens. If the water goes cloudy, you’ve identified a carbonate ion.
Test For Sulfates With HCL?
You can test for sulphate with hydrochloric acid (HCL) and barium chloride (BaCl).
To identify a sulphate ion:
1) Add dilute HCL, followed by barium chloride solution.
2) If a white precipitate of barium sulphate forms, it means the original compound contains a sulphate.
(The hydrochloric acid is added to get rid of any traces of carbonate ions before you do the test. This would also produce a precipitate, so they’d confuse the results).
Litmus Paper Tests For Ammonia Gas?
Ammonia gas (NH3) is alkaline so you can check for it using a damp piece of red litmus paper. If there is ammonia present, the paper will turn blue.
(The litmus paper must be damp so the ammonia gas can dissolve and make the colour change).
Litmus Paper Test For Ammonium Ions?
You can also use the damp litmus paper test for when a substance contains ammonium ions (NH4+):
1) Add some sodium hydroxide to your mystery substance in a test tube and gently heat the mixture.
2) Use litmus paper in the gas that is given off. The litmus paper will turn from red to blue like the test for ammonia gas.
2) If there is ammonia given off, this means there are ammonium ions in your mystery substance.
Testing For Hydroxides Using Litmus Paper?
Litmus paper is also used to test for hydroxides. Testing for hydroxide ions is just the same as testing to see whether a solution is alkaline.
1) Dip a piece of red litmus paper into the solution.
2) If the hydroxide is present, the paper will turn blue.
(Hydroxides aren’t the only alkaline substances so it’s best to use as a test to eliminate the presence of other items first.)
Test For Halides Using Silver Nitrate Solution?
To test for:
- Chloride ions (Cl-),
- Bromide ions (Br-),
- Iodide ions (I-),
1) Add dilute nitric acid (HNO3),
2) Following this, add silver nitrate solution (AagNO3).
Results:
Chloride - white precipitate of silver chloride,
Bromide - cream precipitate of silver bromide,
Iodide - yellow precipitate of silver iodide.
Test For Nitrates With NaOH and Aluminium?
1) To identify nitrate ions, you need to warm the solution of your mystery compound.
2) Add sodium hydroxide solution and aluminium foil to your mystery compound solution.
( The aluminium reduces the nitrate ions to ammonium ions, NH4+ + OH- —> NH3 + H2O).
3) The ammonium ions then reacts with the hydroxide ions to produce ammonia gas and water.
4) So if ammonia is given off, you know your mystery solution must contain nitrate ions. You can test for ammonia gas in the same way as before - with litmus paper.
When Testing For Ions, How Do You Watch For False Positives?
If you’re testing for sulfate ions, you want to make sure that there are no carbonate ions or sulfite ions first - because they will react with the barium chloride. As well as barium sulphate, barium carbonate and barium sulfite are also insoluble. So you will get a false positive and your results wouldn’t mean much at all.
If you’re testing for a halide ions, you want to rule out the presence of sulphate ions first. This is because sulphate ions will also produce a precipitate of silver nitrate. A way of getting round this is, is first add dilute acid to your test solutions. This will get rid of any lurking anions that you don’t want.
Do your tests in this order to avoid mix-ups:
1) Test for carbonates,
2) Test for sulfates,
3) Test for halides.
How to write an electron configuration?
So the first row (helium and hydrogen) is 1s2. This is kinda odd cause helium is in the p-block of the periodic table but it actually has s-orbitals.
Sequence:
1s2, 2s2, 2p6, 3s2, 3p6, 3d10, 4s2, 4p6.
What do the numbers and letter in the electron configuration mean?
1 = This is the number of shells. These numbers are called principal quantum numbers.
S/P/D/F = this is the type of sub-shell. The highest energy sub-shell is the last one in the electron configuration. E.g. 4d2 is a higher electron configuration than 1s2.
S block = there is only one s orbital (s orbitals can only hold 2 electrons on outer shell).
P block = there is 3 p-orbitals in the p block (can only hold 6 electrons on outer shell - 2 in each).
D block = there is 5 d-orbitals in the d block (10 electrons can fit in here - 2 in each).
F block = there are 7 f-orbitals in the f block (14 electrons can fit - 2 in each).
The last little number = the amount of electrons on the outer sub-shell. E.g. 1s1 = there is one electron on the outer shell of the s-orbital.
Shells further from the nucleus (higher energy level) have a greater energy then those closer to the nucleus.
Remember: we fill up p-orbitals a bit differently to a orbitals. The fill up 1 in each, left to right. Then the second electron goes in, left to right again. S orbitals just fill up 2 in each, left to right.
What sub-shell has a lower energy level even thought it’s higher than other sub-shells?
The 4s sub-shell has a lower energy level than the 3d sub-shell even though it’s got a higher principal quantum number.
This means we fill the 4s sub-shell up before we fill the 3d sub-shell up. Confusing, I know.
So when writing configurations, always remember this.
The sequence should go:
1s2, 2s2, 2p6, 3s2, 3p6, 3d10, 4s2.
Remember this when working out ions too. This can get complicated.