Fischer Projection Stereochemistry R S Chirality for one or more chiral centers

March 4, 2020

Leah here from and in this
video I will show you how to find Rns when you’re dealing with a Fischer Projection.
You can find my entire series on Fischer Projections along with my practice quiz and cheat sheets
by visiting my website Now this video is not in in-depth chirality
review but specifically looking at Fischer Projection. So if you’re not comfortable with
how to find r and s, make sure you review that first and then come back to this video.
In video one we look at how to read a Fischer Projection and introduced Mr. Organic Chemistry
which helps you remember that the bow tie or the horizontal lines represent groups coming
out of the page and the vertical lines represent the vertebrae going back and into the page.
You’ll also have to be comfortable ranking your atoms for priority to find r and s and
while there are over a hundred atoms on the periodic table, when it comes to chirality,
I highly recommend memorizing these ten atoms. These are the ten atoms you’ll see over and
over in your Organic Chemistry course and it helps you remember trends such as electronegativity
going up to the right, but more importantly for this, size which goes down to the left. We’re going to rank the atoms in order of
highest atomic number and that’s the specific atom attached to the chiral carbon and then
decreasing. So Iodine will always be your highest then Bromine, then Chlorine, Sulfur,
Phosphorus, then Fluorine, Oxygen, Nitrogen, Carbon and finally Hydrogen will always be
your lowest priority. So looking at this Fischer projection, the
first thing we want to do is rank our groups. When you see Hydrogen, that’s always number
4. Looking at the other atoms we have Bromine as number 1, Oxygen number 2, and Carbon as
number 3. We only care about the top three priorities as long as number 4 is into the
page or on Fischer Projection up or down. Cancel out number 4, trace the path from one
to two to three and since the top of the path goes to the right, that is R. What what happens
when your lowest priority isn’t going into the page? Let’s take a look at the Fischer Projection
for L-Serine. The first thing we want to do is rank the atoms in order of priority. We
recognize Nitrogen to be number one, Hydrogen to be number 4. But then we’re faced with
a carbon and a carbon so what do we do? I’m gonna break it up to show you but this is
something you need to be comfortable doing in your head. The first group we’re looking
at is a carbon double bound to an Oxygen which you want to envision as two bonds to Oxygen,
so I draw out two Oxygen and then another OH, and we’re comparing that to a Carbon bound
to two Hydrogen atoms and then an OH. We start by comparing the Carbons, they’re exactly
the same so we cancel that out. Then we look at the next highest priority on the carbon
atom. For the carboxylic, I can choose any of the three Oxygen atoms that compare to
this Oxygen. once again they’re exactly the same, and cancel out. So we go back to the
Carbon atom and look for the next highest priority. For the carboxylic we have an Oxygen, but
for the alcohol we have just the Hydrogen. Since Oxygen beats Hydrogen, Carboxylic is
going to be priority number 2 and the alcohol will be priority number 3. Now we cross out
number 4 and trace the path from one to two to three which looks like it should be R.
But the problem is, we’re not looking at this correctly because number 4 has to be in the
back and here it’s in the front. You can do different things here like swap, rotate, or
re-draw molecule. But if priority number 4 is directly in the front, just pretend you’re
looking at this backwards. So if looking at it from the front gives me a clockwise or
r-turn, looking at from the back will be exactly the opposite which means I have a counter-clockwise
or s-configuration. L-Serine is in the S configuration. What if you’re given an example that has a
Fischer Projection with two Chiral carbons, you treat it the same way by looking at one
chiral carbon at a time and finding that chirality. So we”ll pick the first chiral carbon and
rank the groups in order of priority. Here’s a quick guide so that you can follow along.
Bromine is priority number 1, Hydrogen is priority number 4, Methyl is 3, that makes
this entire group on the bottom, 2. How did I get that so quickly? Whenever you see Hydrogen,
it’s always, always going to be your absolute lowest priority, make that number4. Whenever
you see a Methyl, it is always going to be your second lowest priority if a Hydrogen
is present. But if there is no Hydrogen present, it will always be your absolute lowest priority
assuming you have no deuterium. So I didn’t even have to look at anything else because
Hydrogen is the lowest, Methyl is the second lowest atom because it has a carbon bound
to the lowest atom hydrogen and so I automatically know that was number 3.
Well let’s say I didn’t know that, what I would have to do is compare what I see. I
have a carbon and that right there is another carbon. They are the same so we have to look
at the next highest priority on that atom. For the methyl group we have Hydrogen, but
for the lower group we have an Oxygen. Since Oxygen beats Hydrogen, the lower portion of
the Fischer Projection outranks the Methyl group which is why the lower portion is two
and the Methyl group is three. Now that we have our priority, cancel out
number 4, trace the path from one to two to three. It looks like it should be R but because
Hydrogen is coming out of the page, remember the bow tie in this Organic Chemistry is coming
forward so you have to reverse it. Look at it from the back and that gives you S. Let’s
do the same thing for the lower carbon. Alcohol is my highest priority that’s one, Hydrogen
is always number 4, Methyl is always behind Hydrogen, number 3. So once again, the rest
of the Fischer projection is number 2. If you didn’t know that, just compare, carbon
to carbon that cancel each other up. The next highest priority in that upper group is that
Bromine and since Bromine outranks Hydrogen, the upper group is 2 and Methyl is 3. And
so we cancel out number 4, trace the path from one to two to three which looks like
it should be R, but because Hydrogen is coming forward, we have to reverse, look at it from
the other side and that means once again we’re dealing with S. But what if you’re still not
comfortable with the structure and want to draw your Fischer as a Sawhorse? or what if
you’re given a sawhorse projection, meaning a three dimensional molecule and you’re asked
to convert that into a Fischer Projection. That’s exactly what I’ll be covering in the
next video which you can catch along with my Fischer Projection cheat sheet and practice
quiz by visiting my website

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