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Polarity
As carbon bonds with atoms of increasing electronegativity, polarity increases.
Alkane
contains single bonds only.
Alkene
An alkene contains a double bond.
Alkyne
An alkyne contains a triple bond.
Structural Isomers
Structural isomers are compounds with the same formula but different structure.
Branching
Increasing branching in hydrocarbons decreases boiling point (BP).
Complete Combustion
Complete combustion produces CO₂ and H₂O.
Hydrogenation
Hydrogenation adds H to remove double bonds.
1-butyne
1-butyne contains a triple bond.
Trans Isomer
Trans isomer means opposite sides.
Alcohol
An alcohol contains an –OH functional group.
Ether
An ether is defined by the structure R–O–R.
Thiol
A thiol contains sulfur instead of oxygen.
Weak Acid
A weak acid is exemplified by phenol.
Dehydration of Alcohol
Dehydration of alcohol gives an alkene.
Secondary Alcohol Oxidation
Secondary alcohol oxidation gives a ketone.
Tertiary Alcohol Oxidation
Tertiary alcohol oxidation does not occur.
Ether Naming
Ether naming involves the format alkyl + alkyl ether.
Oxidation
Oxidation refers to the loss of H or gain of O.
Reduction
Reduction refers to the gain of H.
Carbonyl Group
A carbonyl group is represented as C=O.
Aldehyde
An aldehyde features an end carbonyl.
Ketone
A ketone has a middle carbonyl.
Oxygen Lone Pairs
Oxygen has 2 lone pairs.
Ketone Intermolecular Force
Dipole-dipole interactions are prominent in ketones.
Smaller Ketone
Smaller ketones have increased solubility.
Acetal
An acetal forms from an aldehyde and alcohol.
Hemiacetal
A hemiacetal results from an internal reaction.
Aldehyde Naming
Aldehyde naming uses the suffix –al.
Ketone Naming
Ketone naming uses the suffix –one.
Monosaccharides
Monosaccharides cannot be hydrolyzed.
Aldose
An aldose contains an aldehyde group.
Ketose
A ketose contains a ketone group.
Chiral Carbon
A chiral carbon must have four different groups.
Enantiomers
Enantiomers are mirror images of each other.
Glycosidic Bonds
Glycosidic bonds are ether-like bonds.
Fructose
Fructose is a monosaccharide.
D-Glucose
D-glucose is the most common in nature.
α vs β Glucose
α vs β glucose differ by OH orientation.
Ring Formation in Sugars
Ring formation in sugars occurs by an internal reaction of functional groups.
Butanoic Acid
Butanoic acid is also called butyric acid.
Carboxylic Acids Formation
Carboxylic acids form from primary alcohols by oxidation.
Carboxylic Acids Bonding
Carboxylic acids exhibit hydrogen bonding.
Carboxylic Acid Strength
Compared to strong acids, carboxylic acids are weaker.
Ester Formation
Ester formation involves the reaction of acid and alcohol.
Neutralization Products
Neutralization produces salt and water.
Saponification
Saponification refers to the base hydrolysis of fat.
Solubility and Chain Length
Increasing chain length decreases solubility.
Functional Group
A functional group can be –COOH.
Ester Smell
Esters typically smell fruity.
Triacylglycerol
A triacylglycerol is a fat composed of glycerol and three fatty acids.
Steroids
Steroids consist of four fused rings.
Unsaturated Fatty Acids
Unsaturated fatty acids are bent due to cis double bonds.
Saturated Fats
Saturated fats are solid at room temperature.
Polyunsaturated
Polyunsaturated means containing multiple double bonds.
Saponification Products
Saponification produces soap and glycerol.
Water-soluble Lipids
The most water-soluble lipid is a phospholipid.
Cell Membrane Structure
Cell membrane structure has heads outward and tails inward.
Cholesterol
Cholesterol is classified as a lipid.
Lipids Properties
Lipids are generally nonpolar.
Amines
Amines are classified as bases.
Primary Amine
A primary amine has one carbon attached to nitrogen.
Secondary Amine
A secondary amine has two carbons attached to nitrogen.
Tertiary Amine
A tertiary amine consists of three carbons attached to nitrogen.
Amine Reactions
Amine and acid yield ammonium salt.
Amides Formation
Amides are formed from acid and amine.
Amides Hydrolysis
Amide hydrolysis results in acid and amine.
Amines Boiling Point
Amines have higher boiling points due to hydrogen bonding.
Alkaloids
Alkaloids contain an amine group.
Amine Drugs
Amine drugs are often ammonium salts.
Amino Acids
Amino acids differ by their R group.
Zwitterion
A zwitterion has both positive and negative charges.
Peptide Bond
A peptide bond forms between amino and carboxyl groups.
Primary Structure
Primary structure refers to the sequence of amino acids.
Secondary Structure
Secondary structure includes α-helix and β-sheet.
Tertiary Structure
Tertiary structure refers to the 3D folding of polypeptides.
Quaternary Structure
Quaternary structure involves multiple chains together.
Hemoglobin Structure
Hemoglobin is an example of quaternary structure.
Hydrophobic Interactions
Hydrophobic interactions stabilize tertiary and quaternary structures.
Denaturation Effects
Denaturation affects secondary, tertiary, and quaternary structures.
Enzymes
Enzymes catalyze reactions without being consumed.
Activation Energy
Enzymes lower activation energy to speed up reactions.
Induced Fit
Induced fit describes how enzymes change shape upon substrate binding.
Competitive Inhibitor
A competitive inhibitor binds to the active site.
Noncompetitive Inhibitor
A noncompetitive inhibitor binds to a site different from the active site.
Cofactors
Cofactors are metal ions that assist enzyme function.
Enzyme Suffix
Common suffix for enzymes is –ase.
Low Temperature Effects
Low temperatures slow down enzyme reactions.
Enzyme Effects
Enzymes affect the rate of reactions but not equilibrium.
Isomerase Function
Isomerase enzymes rearrange molecular structure.
Nucleotide Components
A nucleotide contains a base, sugar, and phosphate.
RNA Nucleotide
RNA contains uracil instead of thymine.
DNA Replication
DNA replication uses complementary base pairing.
DNA Strands Orientation
DNA strands are antiparallel.
Transcription
Transcription is the process of synthesizing RNA from DNA.
Translation
Translation is the process of synthesizing protein from RNA.
Codons
Codons code for amino acids during protein synthesis.
Start Codon
The start codon is AUG.
Deletion Mutation
A deletion mutation involves the removal of a base.
Retrovirus
A retrovirus is classified as an RNA virus.