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Chem bio cc 10
ChemBio Lec Perfect
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Chem bio cc 8
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Chem bio cc 4
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Chem bio cc 3
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Cards (164)
Organic Chemistry
Chemistry of
carbon
, from the
interesting
structures that it makes, to the reactions that carbon-containing compounds do
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Organic Chemistry is notorious for being
complicated
because there are so many types of
organic
compounds with unique properties and reactivity
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Organic compounds
Caffeine
in morning tea
Circuitry
in cell phone
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There are over
16
million
known
organic
molecules
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Using basic tools, some practice, and by taking things a step at a time,
organic chemistry
can be learned
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Deboki Chakravarti
Ph.D. in
Biomedical Engineering
, science
writer
/communicator who loves to talk about science
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Much of biomedical engineering is rooted in the
chemistry
of
molecules
, from what they look like to how they interact with each other
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Tools to understand organic chemistry
Bonding
, structure, and naming
molecules
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Molecules
(3S, 8S, 9S, 10R, 13R, 14S,17R)-10, 13 dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[alpha]phenanthren-3-ol (
Cholesterol
)
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Chemists
make observations, do experiments, and propose theories to understand the
chemical
and physical properties of molecules
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Building
molecules
From small molecules like
ethanol
to giant macromolecules like
high-density polyethylene
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Reactions
Elimination
reactions
Substitution
reactions
Pericyclic
reactions
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Practice is required to master
organic chemistry
reactions
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Organic chemistry
is needed to understand
health
, medicine, and the biochemistry of how the body works
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Organic
chemistry can be
complicated
, but with the right approach it can be made sense of
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Oxygen is responsible for life on Earth as we know it, and the fire from combustion reactions is a foundation of civilization
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Atomic
oxygen
is part of water, and adding an
oxygen
atom to organic compounds creates a part of the molecule that's more reactive
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Any heteroatom, which are atoms other than carbon and hydrogen, generally increases the reactivity of organic molecules
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Heteroatoms can make up functional groups, where all the cool chemistry happens
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Steps to naming organic compounds
1. Find the longest carbon chain and give it a root name
2. Identify the highest priority functional group, give it the lowest number on the chain, and add its suffix to the root name
3. Identify any substituents and their positions on the carbon chain, then add a numbered prefix to the root name
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Functional groups
Where all the cool chemistry happens
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Alcohol
A functional group with a structure similar to
water
,
H2O
, but with one of the hydrogens replaced with a carbon chain
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Methanol is super poisonous and usually causes blindness or death, while ethanol is mildly poisonous which causes drunkenness and other health risks
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Numbering carbon chains
To communicate where functional groups are
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Alcohol functional group priority
Has priority over double bonds, triple bonds, and any of the substituents seen so far
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Alcohol compounds
Pentan-1-ol
Pent-2-ene-1-ol
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Ether
A functional group where both hydrogen atoms in
H2O
are replaced with
carbon chains
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The name "ether" refers to one of the first chemicals in medicine that was regularly used to anesthetize patients before surgery
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Trivial name for ether
Names the two carbon chains on either side of the oxygen, adds the suffix -yl, puts them in alphabetical order, and adds "ether" at the end
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Ether compounds
Pentylpropyl ether
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Carbonyl
group
Part of the functional groups found in
aldehydes
, ketones,
carboxylic acids
, and their derivatives
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Aldehyde
Has a carbon chain on only one side of a carbonyl group
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Ketone
Has a carbon chain on both sides of a carbonyl group
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Aldehyde and ketone compounds
Butanal
Propan-2-one (acetone)
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Carboxylic acid
Has an alcohol group on one side of a carbonyl group
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Carboxylic acid compounds
Hex-5-enoic acid
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Carboxylic acids
can undergo reactions to form molecules like esters,
acid chlorides
, anhydrides, and amides
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Amine
A
nitrogen
atom attached to 3 R groups with
one lone
pair, where at least one R group has carbon
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Nitrile
Has a triple bond between a nitrogen atom and a carbon atom, with potential extra stuff hanging off the carbon
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Phenyl
Also known as a benzene ring, a six-carbon ring with alternating single and double bonds
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