Chapter 2 - Professor Welday's Weebly...

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Copyright © 2013 Pearson Education, Inc. Lectures prepared by Christine L. Case © 2013 Pearson Education, Inc. Lectures prepared by Christine L. Case Chemical Principles Chapter 2 1 © 2013 Pearson Education, Inc. The Structure of Atoms Chemistry is the study of interactions between atoms and molecules The atom is the smallest unit of matter that enters into chemical reactions Atoms interact to form molecules 2 © 2013 Pearson Education, Inc. The Structure of Atoms Atoms are composed of Electrons: negatively charged particles Protons: positively charged particles Neutrons: uncharged particles 3 © 2013 Pearson Education, Inc. The Structure of Atoms Protons and neutrons are in the nucleus Electrons move around the nucleus 4

Transcript of Chapter 2 - Professor Welday's Weebly...

Page 1: Chapter 2 - Professor Welday's Weebly Websiteprofwelday.weebly.com/.../2/3/0/0/23005790/ch02_lecture.pdf© 2013 Pearson Education, Inc. Figure 2.1 The structure of an atom.. Electron

Copyright © 2013 Pearson Education, Inc.Lectures prepared by Christine L. Case

© 2013 Pearson Education, Inc. Lectures prepared by Christine L. Case

Chemical Principles

Chapter 2

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The Structure of Atoms

� Chemistry is the study of interactions between atoms and molecules

� The atom is the smallest unit of matter that enters into chemical reactions

� Atoms interact to form molecules

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The Structure of Atoms

� Atoms are composed of� Electrons : negatively charged particles� Protons : positively charged particles� Neutrons : uncharged particles

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The Structure of Atoms

� Protons and neutrons are in the nucleus� Electrons move around the nucleus

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Page 2: Chapter 2 - Professor Welday's Weebly Websiteprofwelday.weebly.com/.../2/3/0/0/23005790/ch02_lecture.pdf© 2013 Pearson Education, Inc. Figure 2.1 The structure of an atom.. Electron

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Figure 2.1 The structure of an atom.

.

Electron shells

Nucleus

Electron (e −)

Neutron (n 0)

Proton (p +)

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� Each chemical element has a different number of protons

� Isotopes of an element are atoms with different numbers of neutrons. Isotopes of oxygen:

816O 8

17O 818O

Chemical Elements 6

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Electronic Configurations

� Electrons are arranged in electron shells corresponding to different energy levels

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Insert Table 2.1

Table 2.1 The Elements of Life 8

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How Atoms Form Molecules

� Atoms combine to complete the outermost shell� The number of missing or extra electrons in this shell

is known as the valence� Molecules hold together because the valence

electrons of the combining atoms form attractive forces, called chemical bonds , between the atomic nuclei

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Chemical Bonds

� A compound contains different kinds of atoms

H2O

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Ionic Bonds

� The number of protons and electrons is equal in an atom

� Ions are charged atoms that have gained or lost electrons

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Figure 2.2a Ionic bond formation.

A sodium atom (Na) loses one electron to an electro n acceptor and forms a sodium ion (Na +). A chlorine atom (Cl) accepts one electron from an ele ctron donor to become a chloride ion (Cl –).

Sodium ion(Na+)

Sodium atom(electron donor)

Chlorine atom(electron acceptor)

Chloride ion(Cl–)

Loss ofelectron

Gain ofelectron

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Ionic Bonds

� Ionic bonds are attractions between ions of opposite charge� One atom loses electrons, and another gains electrons

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Figure 2.2b Ionic bond formation.

The sodium and chloride ions are attracted because of their opposite charges and are held together by an ionic bond to form a molecule of sod ium chloride.

Chloride ion(Cl–)

Sodium ion(Na+)

Sodium chloride moleculeNa+ Cl–

NaCl

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Covalent Bonds

� Covalent bonds form when two atoms share one or more pairs of electrons

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Figure 2.3 Covalent bond formation.

Atomic Diagram

Structural Formula

Molecular Formula A single covalent bond

forms between two hydrogen atoms to form a hydrogen molecule.

Hydrogen atoms

Hydrogen

Hydrogen molecule Carbon

atom

Hydrogen atoms Methane

molecule

Single covalent bonds between four hydrogen atoms and a carbon atom, forming a methane molecule.

Methane

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Hydrogen Bonds

� Hydrogen bonds form when a hydrogen atom that is covalently bonded to an O or N atom is attracted to another N or O atom in another molecule

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Insert Fig 2.4b

Figure 2.4b Hydrogen bond formation in water.

Hydrogenbond

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H2O

2H = 2 ×××× 1 = 2

O = 16

MW = 18

1 mole weighs 18 g

Molecular Weight and Moles

� The sum of the atomic weights in a molecule is the molecular weight

� One mole of a substance is its molecular weight in grams

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Check Your Understanding

� Differentiate an ionic bond from a covalent bond. 2-2

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Learning Objective

Chemical Reactions

2-3 Diagram three basic types of chemical reactions.

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Chemical Reactions

� Chemical reactions involve the making or breaking of bonds between atoms

� A change in chemical energy occurs during a chemical reaction

� Endergonic reactions absorb energy� Exergonic reactions release energy

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� Occur when atoms, ions, or molecules combine to form new, larger molecules

� Anabolism is the synthesis of molecules in a cell

Synthesis Reactions

A + B ABAtom, ion,

or molecule AAtom, ion,

or molecule BNew molecule

AB

Combinesto form

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� Occur when a molecule is split into smaller molecules, ions, or atoms

� Catabolism is the decomposition reactions in a cell

Decomposition Reactions

A + BABAtom, ion,

or molecule AAtom, ion,

or molecule BNew molecule

AB

Breaksdown into

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Exchange Reactions

� Are part synthesis and part decomposition

NaCl + H2ONaOH + HCl

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Reversible Reactions

� Can readily go in either direction� Each direction may need special conditions

A + BWater

ABHeat

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Check Your Understanding� This chemical reaction below is used to remove

chlorine from water. What type of reaction is it? 2-3

HClO + Na2SO3 Na2SO4 + HCl

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Important Biological Molecules

� Organic compounds always contain carbon and hydrogen

� Inorganic compounds typically lack carbon

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Learning Objectives

Inorganic Compounds

2-4 List several properties of water that are important to living systems.

2-5 Define acid, base, salt, and pH.

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Water

� Inorganic� Polar molecule� Solvent

� Polar substances dissociate, forming solutes

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Insert Fig 2.4a

Figure 2.4a Hydrogen bond formation in water. 31

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Insert Fig 2.5

Figure 2.5 How water acts as a solvent for sodium c hloride (NaCl).

Sodium chloride crystal

Sodium iondissolved in water

Chloride iondissolved in water

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Page 9: Chapter 2 - Professor Welday's Weebly Websiteprofwelday.weebly.com/.../2/3/0/0/23005790/ch02_lecture.pdf© 2013 Pearson Education, Inc. Figure 2.1 The structure of an atom.. Electron

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� H+ and OH− participate in chemical reactions

R—R′ + H2O → R—OH + H—R′

Maltose + H2O → Glucose + Glucose

Water 33

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Maltose + H2O → Glucose + Glucose

Glucose C6H12O6

Glucose +C6H12O6

Total C12H24O12

Maltose C12H22O11

The difference is:

Water 34

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Water

� H bonds absorb heat� Makes water a temperature buffer

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Insert Fig 2.4b

Figure 2.4b Hydrogen bond formation in water.

Hydrogenbond

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Insert Fig 2.6

Figure 2.6 Acids, bases, and salts.

Acid Base Salt

HCl NaClNaOH

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Acids

� Substances that dissociate into one or more H+

HCl → H+ + Cl−

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Insert Fig 2.6a

Figure 2.6a Acids, bases, and salts.

Acid

HCl

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Bases

� Substances that dissociate into one or more OH−

NaOH → Na+ + OH−

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Insert Fig 2.6b

Figure 2.6b Acids, bases, and salts.

Base

NaOH

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Salts

� Substances that dissociate into cations and anions, neither of which is H+ or OH−

NaCl → Na+ + Cl−

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Insert Fig 2.6c

Figure 2.6c Acids, bases, and salts.

Salt

NaCl

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Acid-Base Balance

� The amount of H+ in a solution is expressed as pH� pH = −log[H+]� Increasing [H+] increases acidity� Increasing [OH−] increases alkalinity� Most organisms grow best between pH 6.5 and 8.5

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Insert Fig 2.7

Figure 2.7 The pH scale.

pH scale

Stomach acid

Lemon juice

Grapefruit juice

WineTomato juice

UrineMilkPure water

Seawater

Milk of magnesia

Household ammonia

Household bleach

Oven cleanerLimewaterBasic solution

Neutral solution

Acidic solution

Human blood

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Check Your Understanding

� Why is the polarity of a water molecule important? 2-4

� Antacids neutralize acid by the following reaction.

Identify the acid, base, and salt. 2-5

Mg(OH)2 + 2HCl → MgCl2 + H2O

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Learning Objectives

Organic Compounds

2-6 Distinguish organic and inorganic compounds.2-7 Define functional group.

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� The chain of carbon atoms in an organic molecule is the carbon skeleton

Structure and Chemistry 48

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� Functional groups are responsible for most of the chemical properties of a particular organic compound

Structure and Chemistry 49

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Insert Table 2.4(two slides if possible)

Table 2.4 Representative Functional Groups and the Compounds in Which They Are Found (Part 1 of 2) 51

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Insert Table 2.4(two slides if possible)

Table 2.4 Representative Functional Groups and the Compounds in Which They Are Found (Part 2 of 2) 52

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� Identify the functional groups in an amino acid

Functional Groups 53

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Check Your Understanding

� Define organic. 2-6� Add the appropriate functional group(s) to the ethyl

group below to produce each of the following compounds: ethanol, acetic acid, acetaldehyde, ethanolamine, diethyl ether. 2-7

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Learning Objectives

Organic Compounds

2-8 Identify the building blocks of carbohydrates.2-9 Differentiate simple lipids, complex lipids, and

steroids.2-10 Identify the building blocks and structure of

proteins.2-11 Identify the building blocks of nucleic acids.2-12 Describe the role of ATP in cellular activities.

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Organic Compounds

� Small organic molecules can combine into large macromolecules

� Macromolecules are polymers consisting of many small repeating molecules

� The smaller molecules are called monomers

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� Monomers join by dehydration synthesis or condensation reactions

Polymers 58

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Carbohydrates

� Cell structures and energy sources� Consist of C, H, and O with the formula (CH2O)n

� Monosaccharides are simple sugars with three to seven carbon atoms

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Carbohydrates

� Disaccharides are formed when two monosaccharides are joined in a dehydration synthesis

� Disaccharides can be broken down by hydrolysis

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Insert Fig 2.8

Figure 2.8 Dehydration synthesis and hydrolysis.

GlucoseC6H12O6

FructoseC6H12O6

Dehydrationsynthesis

HydrolysisSucroseC12H22O11

Water

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Carbohydrates

� Oligosaccharides consist of 2 to 20 monosaccharides

� Polysaccharides consist of tens or hundreds of monosaccharides joined through dehydration synthesis� Starch, glycogen, dextran, and cellulose are polymers of

glucose that are covalently bonded differently� Chitin is a polymer of two sugars repeating many times

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Check Your Understanding

� Give an example of a monosaccharide, a disaccharide, and a polysaccharide. 2-8

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Lipids

� Primary components of cell membranes� Consist of C, H, and O� Are nonpolar and insoluble in water

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Simple Lipids

� Fats or triglycerides� Contain glycerol and fatty acids; formed by

dehydration synthesis

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Figure 2.9c Structural formulas of simple lipids.

Palmitic acid (saturated)(C15H31COOH)

+

Ester linkage

Molecule of fat (triglyceride)

H2O

H2O

Stearic acid (saturated)(C17H35COOH)

+

cisconfiguration

Oleic acid (unsaturated)(C17H33COOH)

+ H2O

Glycerol

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Simple Lipids

� Saturated fat : no double bonds� Unsaturated fat : one or more double bonds in the

fatty acids� Cis: H atoms on the same side of the double bond� Trans: H atoms on opposite sides of the double bond

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Figure 2.9c Structural formulas of simple lipids.

Palmitic acid (saturated)(C15H31COOH)

+

Ester linkage

Molecule of fat (triglyceride)

H2O

H2O

Stearic acid (saturated)(C17H35COOH)

+

cisconfiguration

Oleic acid (unsaturated)(C17H33COOH)

+ H2O

Glycerol

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Complex Lipids

� Contain C, H, and O + P, N, or S� Membranes are made of phospholipids

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Figure 2.9ab Structural formulas of simple lipids.

Carboxyl group

Hydrocarbon chain

Glycerol

Fatty acid (palmitic acid, Saturated)C15H31COOH

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Steroids

� Four carbon rings with an –OH group attached to one ring

� Part of membranes

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Insert Fig 2.11

Figure 2.11 Cholesterol, a steroid. 73

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Proteins

� Are essential in cell structure and function� Enzymes are proteins that speed chemical reactions� Transporter proteins move chemicals across

membranes� Flagella are made of proteins� Some bacterial toxins are proteins

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Amino Acids

� Proteins consist of subunits called amino acids

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Figure 2.12 Amino acid structure.

Sidegroup

Aminogroup

Carboxylgroup

Generalized amino acid

Cyclicsidegroup

Tyrosine

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Amino Acids

� Exist in either of two stereoisomers : D or L� L-forms are most often found in nature

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Insert Fig 2.13

Figure 2.13 The L- and D-isomers of an amino acid, s hown with ball-and-stick models.

L-amino acid D-amino acid

Left hand Right hand

Mirror78

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Peptide Bonds

� Peptide bonds between amino acids are formed by dehydration synthesis

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Figure 2.14 Peptide bond formation by dehydration s ynthesis.

Glycine Alanine

Dehydrationsynthesis

Peptide bond

Glycylalanine(a dipeptide)

Water

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Levels of Protein Structure

� The primary structure is a polypeptide chain

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Figure 2.15a Protein structure.

Peptide bonds

Primary structure: polypeptide strand (amino acid sequence)

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Levels of Protein Structure

� The secondary structure occurs when the amino acid chain folds and coils in a regular helix or pleats

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Figure 2.15b Protein structure.

Hydrogen bond

Secondary structure:helix and pleated sheet (with three polypeptide strands) Helix

Pleated sheet

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Levels of Protein Structure

� The tertiary structure occurs when the helix folds irregularly, forming disulfide bridges, hydrogen bonds, and ionic bonds between amino acids in the chain

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Figure 2.15c Protein structure.

Disulfidebridge

Tertiary structure: helix and pleated sheets fold into a 3D shape

Hydrogenbond

Disulfide bridge(between cysteine

molecules)

Ionic bond

Details of tertiary structure bonds

Hydrophobic interaction

Polypeptidestrand

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Levels of Protein Structure

� The quaternary structure consists of two or more polypeptides

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Figure 2.15d Protein structure.

Quaternary structure: the relationship of several folded polypeptide chains, forming a protein

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Figure 2.15 Protein structure.

Peptide bonds

Primary structure: polypeptide strand (amino acid sequence)

Hydrogen bond

Secondary structure:helix and pleated sheet (with three polypeptide strands)

Helix

Pleated sheet

Disulfidebridge

Tertiary structure: helix and pleated sheets fold into a 3D shape

Quaternary structure: the relationship of several folded polypeptide chains, forming a protein

Hydrogenbond

Disulfide bridge(between cysteine

molecules)

Ionic bond

Details of tertiary structure bonds

Hydrophobic interaction

Polypeptidestrand

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Levels of Protein Structure

� Conjugated proteins consist of amino acids and other organic molecules� Glycoproteins� Nucleoproteins� Lipoproteins

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Nucleic Acids

� Consist of nucleotides� Nucleotides consist of

� Pentose� Phosphate group� Nitrogen-containing (purine or pyrimidine ) base

� Nucleosides consist of � Pentose� Nitrogen-containing base

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DNA

� Deoxyribonucleic acid� Has deoxyribose� Exists as a double helix� A hydrogen bonds with T� C hydrogen bonds with G

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Insert Fig 2.16

Figure 2.16 The Structure of DNA.

Phosphate Sugar Adenine (A) Thymine (T) Sugar Phosphate

Adenine nucleotide

The carbon atoms in thesugars are identified by adding a marker, ’ (for example, 5’, pronounced “5-prime”). This differentiates them from the carbon atoms in the nucleo-bases, such as Thymine.

Adenine and Thymine (as well as Cytosine and Guanin e, not shown here) are nitrogenous bases or nucleobases.

Hydrogen bonds

Individual DNA nucleotides are composed of a deoxyribose sugar molecule covalently bonded to a phosphate group at the 5’ carbon, and to a nitrogen-containing base at the 3’ carbon. The two nucleotides shown here are held together by hydrogen bonds.

Sugars

PhosphatesSugar-phosphate backbone

The sugar-phosphate backbone of one strand is upside down, or antiparallel, relative to the backbone of the other strand.

DNA double helix

DNA’s double-helical, ladder-like form is made up of many nucleotides base pairs forming the rungs, and the repeating sugar-phosphate combination,forming the backbone.

Thymine nucleotide

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RNA

� Ribonucleic acid� Has ribose� Is single-stranded� A hydrogen bonds with U� C hydrogen bonds with G

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Insert Fig 2.17

Figure 2.17 A uracil nucleotide of RNA.

Phosphate

Uracil (U)

Ribose

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� Adenosine triphosphate� Has ribose, adenine, and three phosphate groups

ATP 96

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Insert Fig 2.18

Figure 2.18 The structure of ATP.

Phosphates

Adenosine

Ribose

Adenine

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� Is made by dehydration synthesis� Is broken by hydrolysis to liberate useful energy

for the cell

ATP 98

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