Section 4: Carbon as The Molecular Basis of Life

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Last updated 8:09 PM on 6/27/26
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SECTION 4 — CARBON: THE MOLECULAR BASIS OF LIFE (IMAT MASTER DECK)

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Why is carbon considered the backbone of life?

It has four valence electrons and can form four stable covalent bonds.

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How many covalent bonds can one carbon atom form?

Four.

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Why is tetravalence important?

It allows carbon to build enormous, stable, complex molecules.

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Can carbon bond to itself?

Yes, forming long chains, branched chains, and rings.

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What types of carbon skeletons exist?

Straight chains, branched chains, rings, and combinations of these.

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Why are carbon-carbon bonds stable?

They are strong covalent bonds.

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Why is carbon more versatile than silicon in biology?

Carbon forms stable bonds at biological temperatures and supports far greater molecular diversity.

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What is an organic molecule?

A molecule containing carbon bonded to hydrogen.

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Are carbon dioxide and carbonates considered organic molecules?

No.

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What is a hydrocarbon?

A molecule composed only of carbon and hydrogen.

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Why are hydrocarbons generally hydrophobic?

C-H bonds are nonpolar.

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What type of bonds are found in saturated hydrocarbons?

Only single covalent bonds.

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What type of bonds are found in unsaturated hydrocarbons?

One or more double or triple bonds.

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What is a saturated fat?

A lipid whose fatty acids contain only single bonds.

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Why are saturated fats usually solid at room temperature?

Straight chains pack tightly together.

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What is an unsaturated fat?

A lipid containing one or more double bonds.

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Why are unsaturated fats usually liquid?

Double bonds create bends that prevent tight packing.

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What is a cis double bond?

Hydrogen atoms are on the same side of the double bond.

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What is a trans double bond?

Hydrogen atoms are on opposite sides of the double bond.

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Which is healthier: cis or trans fats?

Cis fats.

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Why are trans fats associated with cardiovascular disease?

They alter lipid metabolism and increase LDL cholesterol.

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Why can't double bonds rotate freely?

The pi bond restricts rotation.

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What is molecular diversity?

The enormous variety of molecular structures carbon can form.

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Why is molecular shape important?

Shape determines biological function.

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What is an isomer?

Molecules with the same molecular formula but different structures.

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How many major classes of isomers are tested on the IMAT?

Three.

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What are structural (constitutional) isomers?

Same formula but different covalent arrangements.

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What are geometric (cis-trans) isomers?

Same covalent arrangement but different spatial arrangement around a double bond.

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What are enantiomers?

Non-superimposable mirror images.

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What creates an enantiomer?

A chiral carbon bonded to four different groups.

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What is a chiral carbon?

A carbon attached to four different substituents.

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Why are enantiomers biologically important?

Enzymes often recognize only one form.

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Which amino acid configuration is used in proteins?

L-amino acids.

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Which sugar configuration predominates in organisms?

D-sugars.

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Why can two enantiomers have different biological effects?

Proteins and enzymes are themselves chiral.

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What is a functional group?

A group of atoms responsible for characteristic chemical reactions.

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Why do functional groups determine molecular behavior?

They affect polarity, acidity, and reactivity.

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How many functional groups should you know for the IMAT?

Seven.

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What is the hydroxyl group?

–OH.

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Which functional group characterizes alcohols?

Hydroxyl.

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Does the hydroxyl group increase water solubility?

Yes.

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Why does the hydroxyl group increase polarity?

Oxygen is highly electronegative.

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What is the carbonyl group?

C=O.

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Where is the carbonyl group found in aldehydes?

At the end of the carbon skeleton.

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Where is the carbonyl group found in ketones?

Within the carbon skeleton.

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What functional group distinguishes sugars as aldoses or ketoses?

The carbonyl group.

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What is the carboxyl group?

–COOH.

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Why is the carboxyl group acidic?

It can donate H⁺.

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What ion forms when a carboxyl group loses H⁺?

Carboxylate (–COO⁻).

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