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