Carbon and the Molecular Diversity of Life

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Vocabulary flashcards covering Carbon chemistry, functional groups, organic reactions, and the four major classes of biological macromolecules.

Last updated 10:12 PM on 6/10/26
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31 Terms

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Properties of Carbon

Forms 4 covalent bonds (shared electrons); often bonds with O, N, S, H, and P; can form single, double, or triple bonds; molecules may be branched, chains, or rings.

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Isomers

Compounds that have the same molecular formula (numbers and types of atoms) but different structures.

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Structural isomers

A type of isomer where compounds have the same molecular formula but different structural arrangements.

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Geometric isomers

Also known as cis-trans isomers, these have the same molecular formula but vary in spatial arrangement around a double bond.

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Enantiomers

A specific type of isomer characterized by being mirror images of each other.

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Functional groups

Typically two or more different atoms attached to a carbon skeleton that significantly change the structure and function of the molecule.

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Methyl group

A functional group that is non polar (hydrophobic) and neutral.

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Hydroxyl group

A functional group that is polar (hydrophilic) and neutral.

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Carbonyl group

A polar functional group found in carbohydrates such as sugars.

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Carboxyl group

A polar and acidic functional group.

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Amino group

A polar functional group that acts as a base.

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Phosphate group

A functional group that is polar and acidic.

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Sulfhydryl group

A functional group that is polar and neutral.

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Dehydration Synthesis

The joining of two molecules by the removal of water to build larger molecules including polymers; water is produced.

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Hydrolysis

The breaking down of larger molecules into smaller ones by the addition of water; digests polymers into monomers; water is a reactant.

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Lipids

Non polar molecules made of C, H, O, and (P) in phospholipids; not a polymer; functional groups include carboxyl and hydroxyl; examples include fats and steroids.

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Triglycerides

A category of lipids made of one glycerol and 3 fatty acids used for NRT storage.

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Saturated Fats

Animal fats that contain only single CCC - C bonds and are solid at room temperature.

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Unsaturated Fats

Plant and fish fats that contain double CCC - C bonds and are liquid at room temperature.

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Phospholipids

Made of 1 glycerol with a phosphate group and 2 fatty acids; forms the cell membrane.

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Steroids

Lipids made of 4 fused rings; functions include cholesterol in cell membranes and hormones like estrogen and testosterone.

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Carbohydrates

Polymers made of C, H, O, (N) with hydroxyl and carbonyl groups; monomers are monosaccharides bonded by glycosidic linkages; transcript notes: Non polar (will dissolve in water).

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Monosaccharides (simple sugars)

The building blocks of larger molecules with the general formula CH2OCH_2O; examples include Glucose, ribose, deoxyribose, fructose, and galactose.

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Disaccharides

Two monosaccharides bonded together with the formula CnH2n2On1C_nH_{2n-2}O_{n-1}; examples include Sucrose (table sugar), Lactose (milk sugar), and Maltose (beer sugar).

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Polysaccharides

Many monosaccharides bonded together for storage or building; examples include Cellulose (plant walls), Glycogen (animal storage), Starch (plant sugar), and Chitin (exoskeletons).

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Proteins (Polypeptides)

Polymers made of amino acid monomers; contains C, H, O, N, (S) and functional groups like carboxyl and amino; function determined by structure.

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Amino acids

The 20 different monomers of proteins, made different by their specific R groups.

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Primary structure

The sequence of amino acids that make up the polypeptides, held together by peptide bonds.

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Secondary structure

Hydrogen bonding between parts of the backbone components (NCCON - C - C - O); involves components other than the R group.

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Tertiary structure

The overall shape of the polypeptide determined by bonding between R groups, including disulfide bridges, hydrogen bonding, hydrophobic interactions, and ionic bonding.

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Quaternary structure

The overall shape of a protein consisting of 2 or more polypeptide chains; utilizes some bonds found in tertiary structure.