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MCAT::MCAT O. Chem
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seven-charlie-leopard-stairway-bacon-fix
Status
Last Update
Fields
Published
12/12/2023
Specific Rotation Equation
Published
12/12/2023
Structural/Constitutional Isomer
Published
12/12/2023
Stereoisomer
Published
12/12/2023
Conformational Isomer
Published
12/12/2023
Configurational Isomer
Published
12/12/2023
Diasteriomer
Published
12/12/2023
Enantiomer
Published
12/12/2023
Cis
Published
12/12/2023
Trans
Published
12/12/2023
Newman Projection configurations: Least stable to most stable
Published
12/12/2023
The total eclipse configuation has a bond angle of {{c1::0 degrees}} and a {{c2::high}} amount of energy
Published
12/12/2023
The eclipse configuation has a bond angle of {{c1::120 degrees}} and a {{c2::medium}} amount of energy
Published
12/12/2023
The gauche configuation has a bond angle of {{c1::60 degrees}} and a {{c2::low}} amount of energy
Published
12/12/2023
The anti-staggered configuation has a bond angle of {{c1::180 degrees}} and a {{c2::low}} amount of energy
Published
12/12/2023
T or F: Every molecule wants to be in a low energy state
Published
12/12/2023
In the chair conformation, {{c1::axial}} components stick {{c2::up or down}}
Published
12/12/2023
In the chair conformation, {{c1::equatorial}} components stick {{c2::to the side}}
Published
12/12/2023
In the chair conformation, {{c1::wedges}} point {{c2::up}}
Published
12/12/2023
In the chair conformation, {{c1::dashes}} point {{c2::down}}
Published
12/12/2023
What happens when there is interconversion of the chair conformation?
Published
12/12/2023
Chiral
Published
12/12/2023
{{c1::Enantiomers}} have {{c2::same}} physical and chemical properties
Published
12/12/2023
{{c1::Diasteriomers}} have {{c2::different}} physical and chemical properties
Published
12/12/2023
Optical Activity
Published
12/12/2023
{{c1::d+}} rotates light {{c2::clockwise}}
Published
12/12/2023
{{c1::l-}} rotates light {{c2::couterclockwise}}
Published
12/12/2023
Racemic mixture
Published
12/12/2023
T or F: Racemic mixtures are optically active
Published
12/12/2023
Possible number of stereoisomers
Published
12/12/2023
Meso compounds
Published
12/12/2023
{{c1::Meso compounds}} {{c2::are not}} optically active
Published
12/12/2023
What is E/Z configuration used for?
Published
12/12/2023
{{c1::Z}} configuration means the substituents are on {{c2::the same side}} of the double bond
Published
12/12/2023
{{c1::E}} configuration means the substituents are on {{c2::opposite sides}} of the double bond
Published
12/12/2023
Priority values are assigned based on {{c1::atomic number}}
Published
12/12/2023
What is R/S configuration used for?
Published
12/12/2023
{{c1::R}} configuration means the high to low priority substituents are ordered {{c2::clockwise}}
Published
12/12/2023
{{c1::S}} configuration means the high to low priority substituents are ordered {{c2::counterclockwise}}
Published
12/12/2023
T or F: The lowest priority group is placed in the back
Published
12/12/2023
In Fischer projections, the {{c1::horizontal}} lines are {{c2::wedges}} and the {{c1::vertical}} lines are {{c2::dashes}}
Published
12/12/2023
2 ways of inverting the stereochemistry of Fischer projections
Published
12/12/2023
2 ways of retaining the stereochemistry of Fischer projections
Published
12/12/2023
What do you do if the lowest priority group is facing out of the page?
Published
12/12/2023
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12/12/2023
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12/12/2023
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12/12/2023
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12/12/2023
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12/12/2023
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12/12/2023
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12/12/2023
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12/12/2023
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Published
12/12/2023
The highest priority functional group is dependent on what?
Published
12/12/2023
T or F: In cyclic compounds, the triple bond takes priority of the double bond
Published
12/12/2023
Alkane
Published
12/12/2023
Alkene
Published
12/12/2023
Alkyne
Published
12/12/2023
Alcohol
Published
12/12/2023
Aldehyde
Published
12/12/2023
Ketone
Published
12/12/2023
Carboxylic acids
Published
12/12/2023
Ester
Published
12/12/2023
Amide
Published
12/12/2023
Anhydride
Status
Last Update
Fields