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ROB: Well, hello there.
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My name is Rob, and I'm a graduate student at MIT studying plant biology.
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This is the first of many deep dives in 7.00x, where we'll cover topics
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introduced in lecture in greater depth or cover new biological
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problem-solving techniques.
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So this first dive will be how to read a chemical structure.
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Let's dive right in.
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All right.
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I'm showing you the periodic table.
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And you'll notice that certain elements are highlighted in green.
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We've got hydrogen, carbon, nitrogen, oxygen, phosphorous, and sulfur.
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So why did we highlight these?
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These are the most important types of atoms found in biological molecules.
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You'll be seeing quite a bit of them throughout the course, so let's get
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properly acquainted.
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Each of these types of atoms is governed by bonding rules.
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So, for example, let's start with hydrogen.
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Hydrogen likes to form a single bond with another atom.
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We depict it with this line.
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Whereas carbon, carbon prefers to form 4 bonds--
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that means four lines.
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Nitrogen likes to make three bonds, and oxygen likes to make two bonds.
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So using these bonding rules, we can now construct larger molecules or
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combinations of these atoms.
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So let's take a look at one.
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This is a depiction of caffeine, the world's most consumed stimulant.
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You'll notice a couple of types of atoms--
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nitrogens, oxygens--
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but you don't see any carbons or hydrogens.
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But they're definitely there.
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Interesting.
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What's the story here?
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This drawing is a shorthand depiction of the chemical structure.
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Chemists and biologists love using this type of shorthand, but it takes a
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little practice to get used to it.
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There's a couple of rules you have to follow.
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Rule 1 is what I like to call "carbons at the corners." What
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do I mean by that?
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Carbons are found at any corner or the end of any line.
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So for example, corner?
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Carbon.
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End of a line?
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Carbon.
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We can follow that pattern all the way around this molecule.
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Any place where there is a line that doesn't already have an atom depicted
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at the end of it, we know there's a carbon.
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So in this case, we have two, four, six, eight carbons.
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Rule number 2--
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hydrogens bonded to carbons are implied.
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What do I mean by that?
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I mean that these carbons are supposed to be bonded to four different things,
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if you remember our bonding rules.
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And some of these don't have four bonds yet.
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So this one, we can count one, two, three, four--
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it already has all four of its bonds.
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It's following the bonding rules, so it's happy as-is.
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Whereas this carbon, not so much.
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We need to add three bonds to give it its full complement of bonds, and each
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of these bonds will be to a hydrogen atom.
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We can go around and do the same for each of these.
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This one has four.
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It's happy.
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This one has one.
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We need to add three more.
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This one has four.
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This one has four.
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This one has one, so we'll add three.
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This one has one, two, three, and needs a fourth.
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Squeeze that hydrogen right in there.
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Well, look at that.
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All the carbons and hydrogens were actually hiding in plain sight.
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And now you know the way to find them.
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So now we can write out a chemical formula.
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How do we do that?
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We tally up how many atoms of each type make up the molecule.
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In this case, if we count up the carbons, we have eight.
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If we count up the hydrogens, we have 10.
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What about nitrogens?
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I see four.
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Oxygen?
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I see two.
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C8H10N4O2--
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bingo.
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That's our chemical formula.
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So let's take a look at another molecule.
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I'm showing you here the chemical structure for the painkiller aspirin.
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Remembering our rules for carbons and hydrogens, pause the video for a
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moment and try to figure out what the chemical formula is.
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OK.
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Did you come up with your answer?
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Let's go through it together.
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First off, what are the types of atoms that we have here?
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We have a whole bunch of carbons, even though there aren't any Cs visible.
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We have hydrogens, and we have oxygens.
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I can't find any other types of atoms.
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So let's figure out how many carbons we have.
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We have one, two, three, four, five, six, seven, eight, nine
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carbons at the corners.
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Great.
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What about the hydrogens?
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This hydrogen is written out explicitly because it is bonded to an
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oxygen, so we already know that one.
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But all the rest are bonded to carbons, and we have to find them.
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This carbon has four bonds.
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This carbon has four bonds.
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And this carbon has four bonds as well.
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They don't need any hydrogens added.
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This carbon has one, two, three bonds already, so we need a fourth--
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add a hydrogen.
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This carbon has three bonds, so the fourth goes to hydrogen.
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These next two carbons in the ring have three bonds as well, so we'll add
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a single hydrogen to each carbon.
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This one already has four bonds.
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This one needs three additional bonds, so let's add three hydrogens.
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Voila.
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That adds up to one, two, three four, five, six, seven, eight hydrogens.
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So what about the oxygens?
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These are easy.
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Just count them up.
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One, two, three, four.
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Four oxygens.
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You should have gotten C9H8O4 as your chemical formula.
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If you did, bravo.
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Hopefully, you now feel more confident about your ability to read chemical
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structures.
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Going forward, we're going to use our knowledge of chemical structures to
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try and predict how chemicals behave.
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Until next time.
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