Reactions of Organic Functional Groups Part 1: Intro & Acid-Base Review. Circle the functional group that changes in the reaction below.

Similar documents
Chapter 7 Active Reading Guide Cellular Respiration and Fermentation

1. Explain the difference between fermentation and cellular respiration.

Chapter 8: Energy and Metabolism

Alcohols An alcohol contains a hydroxyl group ( OH) attached to a carbon chain. A phenol contains a hydroxyl group ( OH) attached to a benzene ring.

Bioenergetics. Free Energy Change

1. Oxidation number is 0 for atoms in an element. 3. In compounds, alkalis have oxidation number +1; alkaline earths have oxidation number +2.

MULTIPLE CHOICE QUESTIONS

Chem 306 Chapter 21 Bioenergetics Lecture Outline III

Unit Vocabulary: o Organic Acid o Alcohol. o Ester o Ether. o Amine o Aldehyde

CHEMICAL REACTIONS. Chemistry 51 Chapter 6

21.8 The Citric Acid Cycle

What affects an enzyme s activity? General environmental factors, such as temperature and ph. Chemicals that specifically influence the enzyme.

AP BIOLOGY CHAPTER 7 Cellular Respiration Outline

1. The diagram below represents a biological process

Summary of Metabolism. Mechanism of Enzyme Action

Cellular Respiration & Metabolism. Metabolism. Coupled Reactions: Bioenergetics. Cellular Respiration: ATP is the cell s rechargable battery

Chem101: General Chemistry Lecture 9 Acids and Bases

Energy Production In A Cell (Chapter 25 Metabolism)

HOMEWORK PROBLEMS: IR SPECTROSCOPY AND 13C NMR. The peak at 1720 indicates a C=O bond (carbonyl). One possibility is acetone:

1. Enzymes. Biochemical Reactions. Chapter 5: Microbial Metabolism. 1. Enzymes. 2. ATP Production. 3. Autotrophic Processes

EXPERIMENT 1: Survival Organic Chemistry: Molecular Models

Assessment Schedule 2013 Chemistry: Demonstrate understanding of the properties of organic compounds (91391)

Introduction to Biodiesel Chemistry Terms and Background Information

Chapter 6 An Overview of Organic Reactions

These instructions are for a classroom activity which supports OCR A Level Chemistry A.

Alcohols. Copyright 2009 by Pearson Education, Inc. Copyright 2009 Pearson Education, Inc. CH 3 CH 2 CH 2 OH 1-propanol OH

Laboratory 22: Properties of Alcohols

Unit 2 Review: Answers: Review for Organic Chemistry Unit Test

Brønsted-Lowry Acids and Bases

-Loss of energy -Loss of hydrogen from carbons. -Gain of energy -Gain of hydrogen to carbons

Chemistry B11 Chapter 4 Chemical reactions

Chemical Bonds and Groups - Part 1

Organic Functional Groups Chapter 7. Alcohols, Ethers and More

1. The functional group present in carboxylic acids is called a A) carbonyl group. B) carboxyl group. C) carboxylate group. D) carbohydroxyl group.

Acids and Bases: A Brief Review

Survival Organic Chemistry Part I: Molecular Models

Energy & Enzymes. Life requires energy for maintenance of order, growth, and reproduction. The energy living things use is chemical energy.

Cellular Respiration and Fermentation

1. A covalent bond between two atoms represents what kind of energy? a. Kinetic energy b. Potential energy c. Mechanical energy d.

Chapter 4 Chemical Reactions

CH 102 Practice Exam 2 PCC-Sylvania

Anabolic and Catabolic Reactions are Linked by ATP in Living Organisms

Molecules, Compounds, and Chemical Equations (Chapter 3)

Oxidation / Reduction Handout Chem 2 WS11

The correct answer is d C. Answer c is incorrect. Reliance on the energy produced by others is a characteristic of heterotrophs.

ALCOHOLS: Properties & Preparation

CHAPTER 4: Enzyme Structure ENZYMES

19.2 Chemical Formulas

Chapter 2 Polar Covalent Bonds; Acids and Bases

Chemistry Diagnostic Questions

Lecture 15: Enzymes & Kinetics Mechanisms

Figure 5. Energy of activation with and without an enzyme.

Evolution of Metabolism. Introduction. Introduction. Introduction. How Cells Harvest Energy. Chapter 7 & 8

Enzymes and Metabolic Pathways

Chapter 14- RESPIRATION IN PLANTS

Name: Teacher: Pd. Date:

Lab 3 Organic Molecules of Biological Importance

The Citric Acid Cycle

Chapter 7 Cellular Respiration

Cellular Energy: ATP & Enzymes. What is it? Where do organism s get it? How do they use it?

Chapter 2 Polar Covalent Bonds: Acids and Bases

I. ACID-BASE NEUTRALIZATION, TITRATION

Chemical Reactions in Water Ron Robertson

Chemical Bonds. Chemical Bonds. The Nature of Molecules. Energy and Metabolism < < Covalent bonds form when atoms share 2 or more valence electrons.

CHEMISTRY 101 EXAM 3 (FORM B) DR. SIMON NORTH

Chapter 12 Organic Compounds with Oxygen and Sulfur

PRACTICE SET 1. Free energy changes and equilibrium constants

pencil. Vocabulary: 1. Reactant 2. Product 3. Activation energy 4. Catalyst 5. substrate 6. Chemical reaction Keep your textbooks when you are done

Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Two Forms of Energy

18 electron rule : How to count electrons

Microbial Metabolism. Biochemical diversity

Chapter 11. Electrochemistry Oxidation and Reduction Reactions. Oxidation-Reduction Reactions. Oxidation-Reduction Reactions

REVIEW QUESTIONS Chapter 8

Chapter 17. How are acids different from bases? Acid Physical properties. Base. Explaining the difference in properties of acids and bases

Mass Spec - Fragmentation

CHAPTER 15: ANSWERS TO SELECTED PROBLEMS

California State Polytechnic University, Pomona. Exam Points 1. Nomenclature (1) 30

Chemistry 20 Chapters 15 Enzymes

Ch 20 Electrochemistry: the study of the relationships between electricity and chemical reactions.

Chapter 9 Mitochondrial Structure and Function

Cellular Respiration An Overview

4/18/ Substituent Effects in Electrophilic Substitutions. Substituent Effects in Electrophilic Substitutions

Chemical Basis of Life Module A Anchor 2

UNIT (9) CARBOXYLIC ACIDS, ESTERS, AMINES, AND AMIDES

For example: (Example is from page 50 of the Thinkbook)

AP Bio Photosynthesis & Respiration

RESPIRATION AND FERMENTATION: AEROBIC AND ANAEROBIC OXIDATION OF ORGANIC MOLECULES. Bio 171 Week 6

Electrophilic Aromatic Substitution Reactions

RESONANCE, USING CURVED ARROWS AND ACID-BASE REACTIONS

Acids and Bases: Molecular Structure and Acidity

Page Which hydrocarbon is a member of the alkane series? (1) 1. Which is the structural formula of methane? (1) (2) (2) (3) (3) (4) (4)

Ch17_PT MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question.

NET IONIC EQUATIONS. A balanced chemical equation can describe all chemical reactions, an example of such an equation is:

Chemistry and Biochemistry

How To Learn Chemistry And Biochemistry

Cambridge International Examinations Cambridge International Advanced Subsidiary and Advanced Level

Periodic Table Questions

SCH 4C1 Unit 2 Problem Set Questions taken from Frank Mustoe et all, "Chemistry 11", McGraw-Hill Ryerson, 2001

IB Chemistry 1 Mole. One atom of C-12 has a mass of 12 amu. One mole of C-12 has a mass of 12 g. Grams we can use more easily.

Name Lab #3: Solubility of Organic Compounds Objectives: Introduction: soluble insoluble partially soluble miscible immiscible

Transcription:

Reactions of rganic Functional Groups Part 1: Intro & Acid-Base Review Each functional group has unique chemical reactivity. Biological molecules can become very large remember to focus on the functional groups. Most reactions only affect one functional group of a reactant at a time. Recognize the functional groups and look for changes to understand chemical reactivity. Circle the functional group that changes in the reaction below. H H H Almost ALL biochemical reactions are catalyzed by enzymes. What are catalysts? Why do our bodies need enzymes? Draw the Reaction Energy Diagram for a 1-step, exothermic rxn with a large activation energy. verlay another curve showing the rxn with a catalyst.

Acid-Base reactions are the most fundamental & frequent biochemical rxn. Complete the acid-base reactions below. 1) H + ah 2) H H H + HCl H Solubility and Acid-Base Chemistry Classify each functional group and predict water solubility for the reactants and products below. H ah + - a + H 2 H H HCl H H + H Cl - 2

Acid Base Reactions have very low activation energies. ther Biochemical Reactions have larger activation energies. Metabolism: We will study 4 of the biochemical reactions that require catalysts: 1) oxidation-reduction 2) hydration-dehydration 3) acyl group transfer 4) phosphoryl group transfer 3

Reactions of rganic Functional Groups Part 2: Redox Introduction (xidation & Reduction) xidation & Reduction Reactions of Inorganic Molecules Guidelines for Assigning xidation umbers xidation numbers are a way to keep track of electron flow in reactions. The oxidation number is the charge an atom in a compound would have if the electron pairs in each covalent bond belonged to the more electronegative atom. xidation umber Examples Exceptions Pure elements 0 The oxidation numbers for each atom in Fe(s) or 2 is zero. none Fixed charge The oxidation number is equal to Alkali metals +1 Alkaline earth metals +2 none metals its charge. Aluminum +3 F in compounds -1 F in CaF 2 is -1. F in CF 4 is -1. none Cl, Br, & I in compounds -1 if bonded to a less electronegative atom in compounds -2 H in compounds Cl is +1 when bonded with F. Cl is -1 when bonded with Br. in Mg is -2. in H 2 is -2. +1 H in H 2 is +1. none is -1 in peroxides. H is -1 when combined with metals.

Practice recognizing Redox Rxns Balance the following reaction & assign oxidation numbers to each atom. Fe 2 3 + C Fe + C 2 a) Which element is oxidized? b) Which element is reduced? Assign oxidation numbers to each atom in the following reaction. Cu (s) + H 2(g) Cu (s) + H 2 (g) Writing the xidation ½ rxn Writing the Reduction ½ rxn 2

xidation & Reduction of rganic Molecules xidation: Gain bonds to xygen Lose bonds to Hydrogen Reduction: Lose bonds to xygen Gain bonds to Hydrogen Example Breathylzer Test (rganic and Inorganic Redox Combined) H + H 2 Cr 2 7 H + Cr 2 3 Treatment of CH 3 CH 2 CH 2 CH 2 CH with a reducing agent will produce A) an aldehyde. B) a carboxylic acid. C) an alcohol. D) an alkene. E) a ketone. 3

Classify the following reactions as oxidation or reduction. H H For the reactions below, a) Predict the products for the reactions below. Remember: benzene rings are very stable so they will not react. b) Classify each function group. For alcohols, remember to indicate 1, 2, or 3. [H] H [] H [] 4

xidizing Agents: reactant that gets reduced Reducing Agents: reactant that gets oxidized For the following reaction Zn (s) + 2 HCl (aq) Zn 2+ (aq) + H 2(g) + 2 Cl - (aq) a) Write the oxidation half reaction. b) Write the reduction half reaction. c) Which reactant is the oxidizing agent? d) Which reactant is the reducing agent? 5

Reactions of rganic Functional Groups Part 3: Redox of RH & Carbonyls xidation of Alcohols Ethanol Metabolism The oxidation of a 1 alcohol 1

Reduction of Carbonyl Groups Use your knowledge of oxidation reactions to complete the reduction pathways in the following diagram. Classify the functional groups (aldehydes, ketones or alcohols) for the alcohols indicate whether they are 1, 2, 3. In biochemical reactions, reduction of carbonyl groups is carried out by AD + or ADH? 2

Antioxidants ot ALL xidation is Beneficial. xidation reactions form Free Radicals. Antioxidants are substances that trap the odd valence electron to prevent it from causing damage to our biomolecules. xidation from Free Radicals is linked with biological aging. Many antioxidants trap the unpaired electron in an aromatic benzene ring. Vitamin E is an antioxidant. Vitamin E 3

Reactions of rganic Functional Groups Part 4: Hydration-Dehydration Hydration-Dehydration Reactions Hydration of Alkenes Produces Alcohols Dehydration of Alcohols Produces Alkenes Practice reactions. a) + H 2 - H 2 b) + H 2 - H 2 c) step 2 in the break down of fatty acids H 2 SCoA

Reactions of rganic Functional Groups Part 5: Acyl Transfer What is an Acyl Group? Acyl Group Transfer Reactions 2 Pathways Catabolic & Anabolic Acyl Group Hydrolysis Reactions

What happens to carboxylic acids at physiological ph? Draw the structure of acetic acid at physiological ph. The ester for apple flavoring is methyl butanoate. Draw the skeletal-line structure for apple flavoring. Write the hydrolysis reaction for apple flavoring at physiological ph. What happens to amines at physiological ph? Draw ethanamine at physiological ph. Predict the products of the following enzyme catalyzed hydrolysis reactions at physiological ph. H 2 H enzyme 2

Acyl Derivative Formation Add the missing reactants. Show the reaction to form rum flavoring (ethyl formate) using acyl derivative formation. 3

Predict the hydrolysis products of aspartame at physiological ph. 4

Reactions of rganic Functional Groups Part 6: Phosphoryl Grp Transfer What is the effect of physiological ph on phosphate esters? R P H ph 7.4 H Phosphoryl Group Transfer Reactions Phosphate esters are formed when 1 or more of the H atoms of phosphoric acid is (are) replaced with 1 or more R groups. Phosphoanhydride bonds form when the atoms of one phosphate group bonds with the P atom of another phosphate group. Label the Phosphate groups (Pi), Phosphate ester bonds and Phosphoanhydride bonds in the compound below.

Phosphoryl groups play an important role in glycolysis. Glycolysis is the biochemical pathway that breaks down glucose to produce energy. 1 st step of Glycolysis Phosphoryl groups also play a central role in the way energy is transferred in biochemical reactions. ur body stores and transports energy in the phosphoanhydride bonds of ATP. Draw an arrow to the phosphoanhydride bond that is broken and reformed as ATP converts back and forth to ADP. 2

Reactions of rganic Functional Groups Part 7: Coenzymes & Redox Rxns xidation and Reduction reactions ALWAYS occur together. To oxidize or reduce a biological molecule, we need a second compound that can donate or accept the electrons. Coenzymes are the second compound. Coenzymes: special molecules that shuttle electrons Common xidizing and Reducing Agents xidizing Agents Formula or Rxn Bleach acl xygen 2 Hydrogen peroxide H 2 2 Chromium(VI) Cr 6+ Manganese (VIII) Mn - 4 AD + Coenzyme AD + + 2H + + 2e - ADH + H + FAD Coenzyme FAD + 2[H] FADH 2 Reducing Agents Hydrogen H 2 ADPH Coenzyme ADPH + H + ADP + + 2[H] ote the difference

Coenzymes a closer look at the 3 Most Important FAD/FADH 2 FAD is the H Acceptor when C=C (double) bonds form Circle the reactive region of FAD and FADH 2. Diagram the reaction below to indicate the oxidation and reduction ½ reactions. Label each ½ reaction (oxidation or reduction). For the coenzyme, label FAD/FADH 2. H H + + H H 2

AD + /ADH AD + is the H Acceptor in Most xidations Diagram the reaction below to indicate the oxidation and reduction ½ reactions. Label each ½ reaction (oxidation or reduction). For the coenzyme, label AD + /ADH. H + + H ADPH/ADP + ADPH is the H Donor in Reduction Reactions Diagram the reaction below to indicate the oxidation and reduction ½ reactions. Label each ½ reaction (oxidation or reduction). For the coenzyme, label ADPH/ADP +. 3

The reactions for two important pairs of coenzymes are shown below. a) ame them: AD +, ADH, FAD, and FADH 2. Hint: Look closely at the chemical structures to find the differences. b) Label each one of the coenzymes as an oxidizing agent or reducing agent. Reaction 1 a) - P H H H 2 + H 2 H - P H H H H H 2 H 2 P - P - H H H H b) Reaction 2 a) H H H H H H H H H H H P H P H H H 2 H P H P H H H 2 b) 4