Organic compounds do not have to contain only C and H. They can contain other elements such as F, Cl and Br.
Halides A halide is a binary compound, where one part is a halogen atom and the other part is an element, to make it a fluoride, chloride, bromide, iodide, or astatidee compound. These are insoluble in water. Compounds that contain fluoride become unreactive. Compounds that contain CL or Br are mroe reactive but under certain conditions. Compounds that contain I are very reactive.
Nitro Compounds Nitro compounds are organic compounds that contain one or more nitro functional groups. They are often highly explosive especially when the compound contains more than one nitro group and is impure. They are insoluble in water and are unreactive to chemical attacks, except under certain conditions.
Alcohols An alcohol is any compound with an OH group (alcohol group) attached to single bonded hydrocarbons (alkanes). They OH in the alcohol makes this compound soluble in water, but the hydrocarbon chain is still insoluble. All alcohols are poisonous, even the alcohol you drink.
Some compounds may have more than one -OH group. If the ydo, number both and add -diol for 2 and -triol for 3 at the end.
Aldehydes An aldehyde is an organic compound containing a formyl group. This functional group, with the structure R-CHO, consists of a carbonyl center bonded to a hydrogen and an R group. They have double bonded oxygen at the end of a chain.
Ketones
A keytone is a compound with the structure RC(=O)R', where R and R' can be a variety of atoms and groups of atoms. Ketones differ from aldehydes in that the carbonyl is placed between two carbons instead at the end of a carbon.
Alkenes are is the simplest of the unsaturated hydrocarbons, hydrocarbons which will react with hydrogen. They contain one or more double bonds between carbon atoms. They are indicated by the symbol =. The presence of a double bond is indicated when the ending changes from -ane to -ene. The formula for alkenes is CnH2n.
Alkenes
Ethene
C2H4
Propene
C3H6
Butene
C4H8
Pentene
C5H10
Alkynes are hydrocarbons which contain a triple carbon bond. They are indicated by a symbol of 3 lines. The presence of a triple bond is indicated when the ending changes from -ane to -yne. The formula for alkynes is CnH2n-2.
Alkynes
Ethyne
C2H2
Propyne
C3H4
Butyne
C4H6
Pentyne
C5H8
Trans and Cis
Are these two molecules the same? No they are not because no matter how you rotate the molecule, you do not end up with the same molecule. One of these is cis and one of these is trans. Which one is which? The one on the LEFT is trans, because the methyl groups are on the opposite ends. The one on the right is a cis, because the methyl- groups are located on the same side. The molecule on the left is calledtrans-2-butene, while the right one is calledcis-2-butene.
*note* this only applies to alkenes
Organic chemistry, what is that and what do we need it for? Organic chemistry is a subsection of chemistry involving the scientific study of the structure, properties, composition, reactions, and preparations of carbon-based compounds, hydrocarbons, their derivatives. It is what created many of the everyday products that we use.
Organic compounds have low melting points, non-electrolytes and form chains in straight lines, circular patterns or branched patterns. These can be linked up in single, double or triple bonds.
Alkanes are saturated hydrocarbons where all the bonds are single bonds. Each carbon atom forms four bonds and each hydrogen forms a single bond to a carbon. The bonds are tetrahedral which form an angle of 109.5 deg.
Selected Properties of the First 10 Normal Alkanes
Name
Formula
Molar
Masses
Melting
Point (°C)
Boiling
Point (°C)
Number of Structural Isomers
Methane
CH4
16
–183
–162
1
Ethane
C2H6
30
–183
–89
1
Propane
C3H8
44
–187
–42
1
Butane
C4H10
58
–138
0
2
Pentane
C5H12
72
–130
36
3
Hexane
C6H14
86
–95
68
5
Heptane
C7H16
100
–91
98
9
Octane
C8H18
114
–57
126
18
Nonane
C9H20
128
–54
151
35
Decane
C10H22
142
–30
174
75
Formula for writing alkanes: CnH2n+2. Where n = number of carbon atoms.
Hydrocarbons can also have side branches. Branched hydrocarbons are hydrocarbon molecules where the carbon atoms are not arranged in a simple chain, but are arranged in a network of multiple chains.
Naming branched hydrocarbons
Substituent Formula
Number of C Atoms
Name of Substituent
CH3
1
methyl-
CH3CH2
2
ethyl-
CH3CH2CH2
3
propyl-
CH3CH2CH2CH2
4
butyl-
CH3CH2CH2CH2CH2
5
pentyl-
Find and name the longest continuous carbon chain and place it at the end of the name.
Identify and name the groups attached to the chain
Number the chain, starting at the side nearest to the side group
Designate the location of each side group by an appropriate number and name
Assemble the name, listing groups in alphabetical order.
What a loser...puts part 2 and 3 on his website to force you to go there. Well ha! only watch his vids on youtube.
It's the long weekend and my parents are on my tail about not doing any work, so here I am! So lets see...what did we learn this class,OMGWTFBBQ. What is this this thing called electronegativity and polarity.
Electronegativity is a measure of attraction of an atom for electrons in a covalent bond. When 2 different atoms are covalently bonded, they share electrons. This type of bond is polar. Polar bonds result in unequal sharing of electrons in bonds.
Bond types
The difference in electronegativities of 2 elements can be used to predict the natures of bonds. Bonds are categorized into 3 classes:
nonpolar covalent - electrons are shared equally between two atoms
polar covalent - one atom has a greater attraction for electrons than the other atom
ionic - bonding electrons are given away completely to one of the bonding atoms
Predicting Bond Types
When differences are less than 0.5, bonds are considered nonpolar. (0-.04)
When differences are less than 1.7 and greater than 0.5, the bond is covalent. (0.5-1.7)
When differences are 1.7 or greater, the bond is ionic
(1..7 and up)
*wait waaah?? shouldnt it be 1.8? N O. I looked and I kept seeing 1.7 so get over it. *
Eg. What type of bond will HCL be?
H has an electronegativity value of 2.10
CL has an electronegativity value of 3.16
ARE YOU READY FOR THIS?!?! Well im not. Which is why im doing this this blog in the first place. Its time for the Bohr Model. Yeah I know right? This stuff is getting boring but we are almost done. Just 8 more classes, just 8 more classes.
Niels Bohr proposed the Bohr Model in 1915. It is a planetary model where negatively-charged electrons orbit the nucleus. These electrons exist in orbitals and when energy is absorbed, they move to a higher orbital. When energy is lost, electrons fall to a lower orbital.
The Bohr diagrams places the number of neutrons and protons in the center and electrons in energy rings around the outside. Each energy ring has a maximum number it can hold
Ring 1 – 2 electrons
Ring 2 – 8 electrons
Ring 3 – 8 electrons
Ring 4 – 18 electrons
Ring 5 – 18 electrons
Ring 6 – 32 electrons
Ring 7 – 32 electrons
Drawing Bohr Diagrams
Lithium - two of its 3 electrons go into the first level. the third electron goes into the second energy level.
1. Draw a circle and write Li inside of the circle
2. Write the number of protons and neutrons in the circle , which is 3P and 4N
3. Draw an arc which represents the first energy level and label it2e-. This will represent the 2 electrons
in this energy level.
4. Draw a second arc which represents the second energy level and label it 1e- . This represents the third electron.
These will help you on the Lewis structures that were learned in class.
How To Draw Lewis Structures
1) Count the total valence electrons for the molecule: To do this, find the number of valence electrons for each atom in the molecule, and add them up.
2) Figure out how many octet electrons the molecule should have, using the octet rule: The octet rule tells us that all atoms want eight valence electrons (except for hydrogen, which wants only two), so they can be like the nearest noble gas. Use the octet rule to figure out how many electrons each atom in the molecule should have, and add them up. The only weird element is boron - it wants six electrons.
3) Subtract the valence electrons from octet electrons: Or, in other words, subtract the number you found in #1 above from the number you found in #2 above. The answer you get will be equal to the number of bonding electrons in the molecule.
4) Divide the number of bonding electrons by two: Remember, because every bond has two electrons, the number of bonds in the molecule will be equal to the number of bonding electrons divided by two.
5) Draw an arrangement of the atoms for the molecule that contains the number of bonds you found in #4 above: Some handy rules to remember are these:
Hydrogen and the halogens bond once.
The family oxygen is in bonds twice.
The family nitrogen is in bonds three times. So does boron.
The family carbon is in bonds four times.
A good thing to do is to bond all the atoms together by single bonds, and then add the multiple bonds until the rules above are followed.
6) Find the number of lone pair (nonbonding) electrons by subtracting the bonding electrons (#3 above) from the valence electrons (#1 above). Arrange these around the atoms until all of them satisfy the octet rule: Remember,ALL elements EXCEPT hydrogen want eight electrons around them, total. Hydrogen only wants two electrons.
eg. Draw the lewis diagram for
CO2
1) The number of valence electrons is 16. (Carbon has four electrons, and each of the oxygens have six, for a total of 4 + 12 = 16 electrons).
2) The number of octet electrons is equal to 24. (Carbon wants eight electrons, and each of the oxygens want eight electrons, for a total of 8+16 = 24 electrons).
3) The number of bonding electrons is equal to the octet electrons minus the valence electrons, or 8.
4) The number of bonds is equal to the number of bonding electrons divided by two, because there are two electrons per bond. As a result, in CO2, the number of bonds is equal to 4. (Because 8/2 is 4).
5) If we arrange the molecule so that the atoms are held together by four bonds, we find that the only way to do it so that we get the following pattern: O=C=O, where carbon is double-bonded to both oxygen atoms.
6) The number of nonbonding electrons is equal to the number of valence electrons (from #1) minus the number of bonding electrons (from #3), which in our case equals 16 - 8, or 8. Looking at our structure, we see that carbon already has eight electrons around it. Each oxygen, though, only has four electrons around it. To complete the picture, each oxygen needs to have two sets of nonbonding electrons, as in this Lewis structure:
Please note: This video IS super interesting and is ALSO very helpful
Herrroooooo. You guessed it its me again Wes. So about electron configuration...you can do it the bottom, boring, lame super duper hard way. Or you can do it the easy way in the video at the bottom, your choice really. Cheers.
So the first way, which is lame in my opinion is, you write then how the arrows go down. So you start with 1s then 2s then 2p then 3s then 3p then 4s and so on. Remember this: the maximum amount of electrons in each shell are 2 for s, 6 for p, 10 for d, and 14 for f.
A halide is a binary compound, where one part is a halogen atom and the other part is an element, to make it a fluoride, chloride, bromide, iodide, or astatidee compound. These are insoluble in water. Compounds that contain fluoride become unreactive. Compounds that contain CL or Br are mroe reactive but under certain conditions. Compounds that contain I are very reactive.
Nitro Compounds
