SBI4U - Unit 1 Biochemistry

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Chemistry Intro Quiz - 1-27 | Carbs & Lipids Quiz - 28-83

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98 Terms

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List: Four Elements that make up 96% of our body

Carbon, Hydrogen, Oxygen, Nitrogen

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Ionic Bond

Chemical bond formed when one atom gives up electrons, while the other gains them, creating oppositely charged ions that attract each other.

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Covalent Bond

A chemical bond where two atoms share one or more pairs of electrons.

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Polar Covalent Bond

A covalent bond where electrons are shared unequally, creating slight positive and negative charges on the atoms.

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Polarity

A property of a molecule where one end is slightly positive and the other end is slightly negative due to unequal sharing of electrons.

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Bonding Capacity

The number of chemical bonds an atom can form

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Electronegativty

The strength of the hold an atom has on electrons

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Dipole

A separation of electrical charge in a molecule due to an uneven sharing of electrons, resulting in a partial positive & partial negative.

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VSEPR theory

Theory that predicts the shape of a molecule based on: Valence Shell, Electron Pairs, Repulsion.

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Cohesion

The attraction between like molecules that holds them together.

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Adhesion

The attraction between molecules of different substances that causes them to stick together

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Hydrophobic

Repels water, refers to non-polar molecules

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Hydrophilic

Attracts water, refers to polar molecules

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Hydroxyl Group

Functional group with the chemical formula -OH. Referred to as alcohols and they are polar due to electronegativity difference between O and H.

<p>Functional group with the chemical formula -OH. Referred to as alcohols and they are polar due to electronegativity difference between O and H.</p>
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Carbonyl Group (Aldehydes)

Functional group with the chemical formula -COH, where C=O (double bond). Referred to as aldehydes and they are polar.

<p>Functional group with the chemical formula -COH, where C=O (double bond). Referred to as aldehydes and they are polar.</p>
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Carbonyl Group (Ketones)

Functional group with the chemical formula -CO-, where C=O (double bond). Referred to as ketones and are polar.

<p>Functional group with the chemical formula -CO-, where C=O (double bond). Referred to as ketones and are polar.</p>
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Carboxyl Group

Functional group with the chemical formula -COOH, where C=O (double bond). Referred to as carboxylic acids and are polar.

<p>Functional group with the chemical formula -COOH, where C=O (double bond). Referred to as carboxylic acids and are polar.</p>
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Amino Group

Functional group with the chemical formula -NH2. Referred to as amines and are polar.

<p>Functional group with the chemical formula -NH2. Referred to as amines and are polar.</p>
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Sulfhydryl Group

Functional group with the chemical formula -SH. Referred to as thiols and are slightly polar.

<p>Functional group with the chemical formula -SH. Referred to as thiols and are slightly polar.</p>
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Phosphate Group

Functional group with the chemical formula -PO4. Referred to as organic phosphates and are polar.

<p>Functional group with the chemical formula -PO4. Referred to as organic phosphates and are polar.</p>
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London Dispersion Forces

Weak and non-polar intermolecular force created by temporary attraction of electrons from one molecule to the nucleus of another nearby molecule. This is present in all molecules.

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Dipole-Dipole Forces

Weak but polar intermolecular force between a positive dipole of one molecule and a negative dipole of another molecule. Present in two polar molecules.

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Hydrogen Bonds (THE FORCE)

A special strong type of dipole-dipole force that occurs when a hydrogen atom bonds to a highly electronegative atom (N, O or F).

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Bent Molecular Geometry

The shape of a polar molecule where a central atom is bonded to two other atoms and has one or more lone pairs.

<p>The shape of a polar molecule where a central atom is bonded to two other atoms and has one or more lone pairs.</p>
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Linear Molecular Geometry

The shape of a non-polar molecule where the central atom is bonded to two other atoms with no lone pairs.

<p>The shape of a non-polar molecule where the central atom is bonded to two other atoms with no lone pairs.</p>
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Tetrahedral Molecular Geometry

The shape of a non-polar molecule where a central atom is bonded to four other atoms with no lone pairs.

<p>The shape of a non-polar molecule where a central atom is bonded to four other atoms with no lone pairs.</p>
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Trigonal Pyramid Molecular Geometry

The shape of a polar molecule where a central atom is bonded to three other atoms and has one lone pair.

<p>The shape of a polar molecule where a central atom is bonded to three other atoms and has one lone pair.</p>
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Biological Molecules

Macromolecules that are composed of repeating subunits

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List: The Four Biological Molecules

Carbohydrates, lipids, proteins, nucleic acids

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Carbohydrates

A macromolecule that s made up of one or many sugar molecules. They contain C, H & O atoms only and are in a 1:2:1 ratio. They end in -saccharide or -ose.

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List: Five Functions of Carbohydrates

  1. Energy Source

  2. Building Materials

  3. Cell-to-cell communication

  4. Blood Glucose Level Regulation

  5. Fibre for waste elimination

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Monosaccharide

A carbohydrate referred to as “simple sugars.” They have single chains of C atoms with hydroxyl groups. They can be distinguished by # of C atoms in their backbone and their specific carbonyl group.

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Glucose

An example of a monosaccharide with the chemical formula C6H12O6 and a hexagon ring structure. It is used within cells as energy.

<p>An example of a monosaccharide with the chemical formula C6H12O6 and a hexagon ring structure. It is used within cells as energy.</p>
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Fructose

An example of a monosaccharide with the chemical formula C6H12O6 and a pentagon ring structure. It is found in fruits.

<p>An example of a monosaccharide with the chemical formula C6H12O6 and a pentagon ring structure. It is found in fruits.</p>
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Monomers

Small, single molecules that join together to form polymers

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Polymers

A large molecule made up of many monomers bonded together

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Isomers

Molecules with the same chemical formula but with different structural arrangement of atoms

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Pentoses

Monosaccharides with five C atoms in the backbone

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Hexoses

Monosaccharides with six C atoms in the backbone

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Ribose

An example of a pentose found in RNA

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Ribulose

An example of a pentose used in photosynthesis

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Galactose

An example of a monosaccharide that is found in dairy products.

<p>An example of a monosaccharide that is found in dairy products.</p>
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Ring Structure of Monosaccharides

This structure is obtained when the monosaccharide is immersed in water, as the C-5 & C-6 atoms react with the carbonyl group by dissolving to form a closed ring.

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Chain Structure of Monosaccharides

This structure is obtained when the monosaccharide is in a dry state

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α-glucose

A form of glucose that has the hydroxyl group on C-1 pointing down. It forms starch (in plants) and glycogen (in animals), both of which humans can digest for energy.

<p>A form of glucose that has the hydroxyl group on C-1 pointing down. It forms starch (in plants) and glycogen (in animals), both of which humans can digest for energy.</p>
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β-glucose

A form of glucose that has the hydroxyl group on C-1 pointing up. It forms cellulose, which humans cannot digest for energy.

<p>A form of glucose that has the hydroxyl group on C-1 pointing up. It forms cellulose, which humans cannot digest for energy.</p>
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Disaccharides

A carbohydrate that consists of two simple sugars (monomers) bonded together.

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Dehydration Synthesis

A process in which two monomers bond together to form a polymer by removing a water molecule in the process. Also called a condensation reaction.

<p>A process in which two monomers bond together to form a polymer by removing a water molecule in the process. Also called a condensation reaction.</p>
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Anabolic Reactions

Reactions that build larger molecules from smaller subunits, requiring energy input

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Catabolic Reactions

Reactions that break down larger molecules into smaller subunits, where H2O molecules are used to break covalent bonds, releasing energy output.

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Hydrolysis

A process in which a polymer is broken down into two monomers by adding a water molecule.

<p>A process in which a polymer is broken down into two monomers by adding a water molecule.</p>
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Maltose

An example of a disaccharide that is found in beer. Made up of glucose + glucose.

<p>An example of a disaccharide that is found in beer. Made up of glucose + glucose.</p>
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Sucrose

An example of a disaccharide that is found as table sugar. Made up of glucose + fructose.

<p>An example of a disaccharide that is found as table sugar. Made up of glucose + fructose.</p>
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Lactose

An example of a disaccharide that is found in milk. Made up of α or glucose + galactose.

<p>An example of a disaccharide that is found in milk. Made up of α or glucose + galactose.</p>
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Glycosidic Linkage

A covalent bond that joins two monosaccharides together through an oxygen atom, created by dehydration synthesis.

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Polysaccharides

A very complex form of carbohydrate that is made up of 100s or 1000s of subunits held together by glycosidic linkages.

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Starch

An example of a polysaccharide that is formed by linking excess α-glucose produced by plants, which they use to store energy. It is made up of amylose and amylopectin.

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Amylose

An example of a polysaccharide that makes up starch. They are chains of coiled α-glucose monomers in a straight chain with α1-4 glycosidic linkages.

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Amylopectin

An example of a polysaccharide that makes up starch. They are chains of coiled α-glucose monomers with α1-4 glycosidic linkages, AND it has branching α-glucose monomers to the main chain by α1-6 glycosidic linkages.

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Glycogen

An example of a polysaccharide that is used by animals to store energy. It is similar to amylopectin, but it has more branches of α-glucose monomers at α1-6. Their stores are depleted after a day of not being used.

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Cellulose

An example of a polysaccharide that is a polymer of β-glucose monomers, rather than α-glucose in amylose. The β-glucose monomers are connected by β1-4 glycosidic linkages. It is not coiled, since every second glucose monomer is inverted, creating a straight chain that has no coils. Humans lack the enzyme necessary to break down the linkages of this polysaccharide.

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Lipids

A macromolecule that contains mainly C-H bonds. They do not mix well with water, as they are hydrophobic.

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List: Four Functions of Lipids

  1. Energy Storage

  2. Insulation

  3. Building cell membranes

  4. Sending cell signals

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List: Four Types of Fats

  1. Fats

  2. Phospholipids

  3. Steroids

  4. Waxes

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Fats

A type of lipid that is mainly used for energy storage. Excess carbs are converted into fats and stored in adipose tissue

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Adipose Tissue

Tissue where excess carbs are converted into fats and stored in

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Triglyceride

The most common fat that is made up of a glycerol backbone and three fatty acid chains connected by an ester linkage.

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Ester Linkage

A covalent bond formed between a hydroxyl group of glycerol and a carboxyl group of a fatty acid. Used to build triglycerides.

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Fatty Acids

Long, hydrocarbon chains with a carboxyl group at the end

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Saturated fats

Fsts that only contain single C-C bonds. They are solid at room temperature and mostly found in animals

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Unsaturated fats

Fats that contain one C=C bond (monounsaturated) or multiple C=C bonds (polyunsaturated). They are liquid at room temperature and mostly found in plants

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Kinks

Refers to the bends in a fatty acid chain caused by double bonded C=C atoms.

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“Bad Fats”

Refers to saturated fats since they accumulate in the blood vessels easily, causing plaques and leading to heart disease

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Hydrogenation

Process by which H bonds and added, breaking the C=C bonds and creating a solid from a liquid.

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Cis Fats

Refers to unsaturated fats where the hydrogen atoms attached to a double C=C bond are on the same side.

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Trans Fats

Refers to unsaturated fats where the hydrogen atoms attached to a double C=C bond are on opposite sides.

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Phospholipids

A type of lipid that are the main component of cell membranes. They form a bilayer, and have hydrophobic heads facing outward and hydrophobic tails facing inward. They are made up of 2 fatty acids, a glycerol molecule, a phosphate and a polar molecule.

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Steroids

A type of lipid that are hydrophobic and contain 4 fused rings with functional groups.

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Cholesterol

A type of steroid that maintains rigidity & fluidity in the cell membrane. They travel in the bloodstream as lipoproteins.

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HDL Cholesterol

A type of cholesterol that is a highly dense lipoprotein. They are the good cholesterol, as they remove excess LDL building up in the body. Cis-unsaturated fats trigger the synthesis of it.

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LDL Cholesterol

A type of cholesterol that is a lowly dense lipoprotein. They are the bad cholesterol, as they build plaques in the bloodstream, leading to heart disease. Saturated fats trigger the synthesis of it, and trans fats trigger even more synthesis.

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Lipoprotein

A combination of lipids & proteins

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Waxes

A type of lipid that are long fatty acid chains with alcohol & carbon rings. They are hydrophobic.

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List: Six Functions of Proteins

  1. Cell signaling

  2. Transport

  3. Storage

  4. Biological catalysts

  5. Structure

  6. Movement

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Proteins

A type of macromolecule that is made up of an amino acid molecule held together by a peptide bond to for a polypeptide chain.

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Peptide Bond

The bond that holds together amino acids, where the carboxyl group of one AA react with the amino group of another AA

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Amino Acids

The building blocks of proteins that are made up of an amino group, a carboxyl group and a side chain. There are 20 amino acids.

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Essential Amino Acids

8 of the 20 amino acids that humans do not produce, and need to intake as food.

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Globular Proteins

Proteins that are described in terms of four different structural levels

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Primary Structure

The structural level that refers to the sequence of amino acids in a polypeptide chain

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Secondary Structure

The structural level that refers to the folding/coiling that occurs as more AA’s are added to a chain. They consist of alpha-helices and beta-pleated sheets.

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Alpha-Helices

A secondary protein structure that is formed when the O in the carboxyl group (C=O) reacts with the H in the amino group (N-H) in an amino acid that is 4 peptide bonds away

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Beta-Pleated Sheets

A Secondary protein structure that is formed when 2 parts of the polypeptide chain lie parallel to each other, allowing H-bonds to form between O atoms in the carboxyl group of one AA to the H atoms in the amino group of another AA.

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Tertiary Structure

The structural level that refers to the additional folding occurring between AA’s in a polypeptide due to external environment to create a functional protein. Bonds can affect the tertiary structure.

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List: Four Bods that affect tertiary structure

  1. Hydrogen Bonding between polar R groups

  2. Ionic Bonding between acidic/basic R groups

  3. Disulfide bridges (-S-S-) between 2 cysteines

  4. Other Intermolecular Forces

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Quaternary Structure

A structural level that refers to when 2 or more polypeptides come together to form a functional protein. This does not always happen.

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Protein Denaturation

A process in which the bonds holding a protein in its tertiary structure can break, causing the polypeptide to unravel.

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List: Four Causes of Protein Denaturation

  1. Heat

  2. pH

  3. Salinity

  4. Physical Forces