CHEM-1020: Introduction to Organic Chemistry and Biochemistry 1

Total Page:16

File Type:pdf, Size:1020Kb

CHEM-1020: Introduction to Organic Chemistry and Biochemistry 1 CHEM-1020: Introduction to Organic Chemistry and Biochemistry 1 CHEM-1020: INTRODUCTION TO ORGANIC CHEMISTRY AND BIOCHEMISTRY Cuyahoga Community College Viewing: CHEM-1020 : Introduction to Organic Chemistry and Biochemistry Board of Trustees: 2018-11-30 Academic Term: Fall 2021 Subject Code CHEM - Chemistry Course Number: 1020 Title: Introduction to Organic Chemistry and Biochemistry Catalog Description: Structure and properties of representative carbon compounds and applications to everyday life. Nature and metabolism of biochemical compounds and relationship of nucleic acids to protein synthesis. Credit Hour(s): 4 Lecture Hour(s): 3 Lab Hour(s): 3 Other Hour(s): 0 Requisites Prerequisite and Corequisite CHEM-1010 Introduction to Inorganic Chemistry, or CHEM-101H Honors Introduction to Inorganic Chemistry, or sufficient score on Chemistry Assessment test. Outcomes Course Outcome(s): Apply basic principles of organic chemistry to health careers or other advanced scientific studies. Essential Learning Outcome Mapping: Critical/Creative Thinking: Analyze, evaluate, and synthesize information in order to consider problems/ideas and transform them in innovative or imaginative ways. Objective(s): 1. Name organic compounds including alkanes, alkenes, aromatic, aldehydes, ketones, carboxylic acids, amines, amides, esters, ethers, alcohols, and thiols using International Union of Pure and Applied Chemistry (IUPAC) nomenclature and common names. 2. Compare the structures, formulas, and properties of organic molecules. 3. Relate the stucture and function of organic molecules as inhibitors of enzymes. Course Outcome(s): Apply a fundamental knowledge of biochemistry when working in the health sciences or in other advanced scientific studies. 2 CHEM-1020: Introduction to Organic Chemistry and Biochemistry Essential Learning Outcome Mapping: Critical/Creative Thinking: Analyze, evaluate, and synthesize information in order to consider problems/ideas and transform them in innovative or imaginative ways. Objective(s): 1. Describe protein metabolism including the relationships to the citric acid cycle, the urea cycle, and gluconeogenesis. 2. Define the nature and properties of hormones and other chemical messengers 3. List the nature and properties of lipids including simple and compound lipids and steroids along with the relationship to cell membranes. 4. Describe the nature of digestion including the related enzymes and the resultant blood sugar levels along with the processes of glycogenesis and glycogenolysis. 5. Interrelate carbohydrate, lipid, and protein metabolisms, the effects of fasting, and the causes of positive and negative protein balance. 6. Describe the nature and properties of amino acids and proteins including zwitterion structure, amphoteric nature, isoelectric point, optical activity of amino acids and the primary, secondary, tertiary, and quaternary structures of proteins. 7. Explain the nature and properties of enzymes including the composition, specificity, various functions, and inhibition. 8. Compare the composition and nature of DNA and RNA and explain the relationship of DNA and RNA to protein synthesis. 9. List the nature and properties of carbohydrates including monosaccharides, disaccharides and polysaccharides 10. Examine carbohydrate metabolism including glycolysis, the citric acid cycle, and the electron transport chain with the resultant production of adenosine triphosphate (ATP) from adenosine diphosphate (ADP). 11. Relate lipid metabolism including the beta oxidation cycle of fatty acids with the citric acid cycle and the electron transport chain and the ATP calculation for a given fatty acid. Course Outcome(s): Apply laboratory safety and fundamental laboratory skills to health careers and other scientific studies. Essential Learning Outcome Mapping: Critical/Creative Thinking: Analyze, evaluate, and synthesize information in order to consider problems/ideas and transform them in innovative or imaginative ways. Objective(s): 1. Demonstrate laboratory safety and fundamental laboratory skills and techniques. 2. Construct ball and stick models for the organic functional groups and cis-trans isomers as well as o,p,m isomers to determine three-dimensional nature of organic molecules. 3. Deduce the structures of organic molecules using representative chemical tests. 4. Distinguish between biomolecules such as amino acids, proteins, carbohydrates, lipids, and fatty acids using chemical tests. Course Outcome(s): Apply fundamental knowledge of organic chemistry and biochemistry to communicate scientific information in written formats. Essential Learning Outcome Mapping: Written Communication: Demonstrate effective written communication for an intended audience that follows genre/disciplinary conventions that reflect clarity, organization, and editing skills. Objective(s): 1. Report experimental results and conclusions in a written form 2. Use information resources in chemistry, including the primary literature, and report in a written form Methods of Evaluation: 1. Exams 2. Final examination 3. Laboratory exam(s) 4. Quizzes 5. Written Lab reports 6. Subjective evaluation of laboratory skills by the instructor 7. Participation 8. Homework assignments 9. Research paper/report CHEM-1020: Introduction to Organic Chemistry and Biochemistry 3 Course Content Outline: 1. Saturated hydrocarbons a. Classification of organic compounds according to functional groups b. Alkanes and cycloalkanes c. System of naming (nomenclature) devised by International Union of Pure and Applied Chemistry (IUPAC) d. Properties and reactions of satuarated hydrocarbons e. Safety in organic chemistry laboratory f. Chemical model building g. Experimental procedures for analysis of organic compounds 2. Unsaturated hydrocarbons a. Alkenes, alkynes and aromatic compounds b. Nomenclature by IUPAC method c. CIS-trans isomerism, addition polymers and benzene d. Properties and reactions e. Experimental evaluation of the reactivity of different hydrocarbons f. Synthesis of a polymer g. study of polymer solubility 3. Alcohols, phenols, ethers a. Nomenclature by IUPAC method and some common names b. Physical and chemical behavior c. Observation of their properties and reactivity 4. Organic halogen and sulfur compounds a. Nomenclature b. Disulfides c. Uses of halogenated compounds 5. Aldehydes and ketones a. Nomenclature by IUPAC method and some common names b. Physical and chemical behavior c. Observation of properties and reactivity 6. Carboxylic acids and their derivatives a. Esters and amides b. Nomenclature by IUPAC method and some common names c. Physical and chemical behavior d. Observation of properties and reactivity e. Synthesis of aspirn f. Technique of thin layer chromatography 7. Amines a. Nomenclature by IUPAC method and some common names b. Properties and reactions c. Heterocyclic nitrogen compounds and alkaloids 8. Amino acids and proteins a. Introduction to biochemistry b. Amino acids classification c. Physical and chemical properties of amino acids d. Handedness in amino acids e. Peptide bond f. Dipeptides, tripeptides, and polypeptides g. Protein structure i. primary ii. secondary iii. tertiary iv. quaternary h. Protein hydrolysis and protein denaturation i. Experimental tests on amino acids and proteins to determine properties and reactivity 9. Enzymes, vitamins, and chemical messengers a. Catalysis by enzymes b. Enzymes structure c. Models of enzyme action 4 CHEM-1020: Introduction to Organic Chemistry and Biochemistry d. Effects of concentration, temperture and pH on enzyme activity e. Enzyme regulation f. Water soluble vitamins g. Fat soluble vitamins h. Antioxidants i. Hormones j. Neurotransmitters and drugs k. Laboratory study of several enzymes 10. Nucleic acids and protein synthesis a. Composition of nucleic acids and structure of the chains b. The Watson-Crick model c. Replication of DNA d. Structure and function of RNA e. Transcription f. The Genetic code g. Translation 11. Carbohydrates a. Handedness b. The D and L family of sugars c. Monosaccharide, disaccharides and plysaccharides: structures and reactions d. Experimental tests on carbohydrates 12. Lipids a. Structure and classification b. Fatty acides c. Esters of fatty acids d. Fats and oils e. Hydrogenation reaction of oils f. Hydrolysis of fats and oils g. Cell membrane lipids h. Structure of cell membranes i. Transport across cell membranes j. Experimentation on the process of soap and detergent production 13. Metabolism of carbohydrates, lipids, and proteins a. Overview of metabolism and energy production b. Metabolic pathways c. Oxidized and reduced coenzymes d. The citric acid cycle e. The Electron-transport chain and ATP production f. Digestion of carbohydrates, triacylglycerols and proteins g. Glycolysis, glycogenesis, glycogenolysis and gluconeogenesis h. Glycerol catabolism i. Oxidation of fatty acids j. The urea cycle k. Catabolism of the carbon skeleton of amino acids l. Catabolism of heme Resources McMurry, John, Mary Castellion, David S. Ballantine, Carl A. Hoeger, and Virginia E. Peterson. Fundamentals of General, Organic and Biological Chemistry. 8th ed. Upper Saddle River, NJ: Prentice-Hall, 2016. Smith, Janice G. General, Organic, and Biological Chemistry. 3rd ed. New York: McGraw-Hill, 2016. Bettelheim, Frederick A., William H. Brown, Mary K. Campbell, and Shawn O. Farrell. Introduction to General, Organic, and Biochemistry. 11th ed. Belmont: Brooks/Cole, 2015. Seager, S.; Slabaugh, M.; Hansen, M. Chemistry for Today: General, Organic, and Biochemistry. 9th
Recommended publications
  • Prebiological Evolution and the Metabolic Origins of Life
    Prebiological Evolution and the Andrew J. Pratt* Metabolic Origins of Life University of Canterbury Keywords Abiogenesis, origin of life, metabolism, hydrothermal, iron Abstract The chemoton model of cells posits three subsystems: metabolism, compartmentalization, and information. A specific model for the prebiological evolution of a reproducing system with rudimentary versions of these three interdependent subsystems is presented. This is based on the initial emergence and reproduction of autocatalytic networks in hydrothermal microcompartments containing iron sulfide. The driving force for life was catalysis of the dissipation of the intrinsic redox gradient of the planet. The codependence of life on iron and phosphate provides chemical constraints on the ordering of prebiological evolution. The initial protometabolism was based on positive feedback loops associated with in situ carbon fixation in which the initial protometabolites modified the catalytic capacity and mobility of metal-based catalysts, especially iron-sulfur centers. A number of selection mechanisms, including catalytic efficiency and specificity, hydrolytic stability, and selective solubilization, are proposed as key determinants for autocatalytic reproduction exploited in protometabolic evolution. This evolutionary process led from autocatalytic networks within preexisting compartments to discrete, reproducing, mobile vesicular protocells with the capacity to use soluble sugar phosphates and hence the opportunity to develop nucleic acids. Fidelity of information transfer in the reproduction of these increasingly complex autocatalytic networks is a key selection pressure in prebiological evolution that eventually leads to the selection of nucleic acids as a digital information subsystem and hence the emergence of fully functional chemotons capable of Darwinian evolution. 1 Introduction: Chemoton Subsystems and Evolutionary Pathways Living cells are autocatalytic entities that harness redox energy via the selective catalysis of biochemical transformations.
    [Show full text]
  • Organic Chemistry PEIMS Code: N1120027 Abbreviation: ORGCHEM Number of Credits That May Be Earned: 1/2-1
    Course: Organic Chemistry PEIMS Code: N1120027 Abbreviation: ORGCHEM Number of credits that may be earned: 1/2-1 Brief description of the course (150 words or less): Organic chemistry is an introductory course that is designed for the student who intends to continue future study in the sciences. The student will learn the concepts and applications of organic chemistry. Topics covered include aliphatic and aromatic compounds, alcohols, aldehydes, ketones, acids, ethers, amines, spectra, and stereochemistry. A brief introduction into biochemistry is also provided. The laboratory experiments will familiarize the student with the important laboratory techniques, specifically spectroscopy. Traditional high school chemistry courses focus on the inorganic aspects of chemistry whereas organic chemistry introduces the student to organic compounds and their properties, mechanisms of formations, and introduces the student to laboratory techniques beyond the traditional high school chemistry curriculum. Essential Knowledge and Skills of the course: (a) General requirements. This course is recommended for students in Grades 11-12. The recommended prerequisite for this course is AP Chemistry. (b) Introduction. Organic chemistry is designed to introduce students to the fundamental concepts of organic chemistry and key experimental evidence and data, which support these concepts. Students will learn to apply these data and concepts to chemical problem solving. Additionally, students will learn that organic chemistry is still evolving by reading about current breakthroughs in the field. Finally, students will gain appreciation for role that organic chemistry plays in modern technological developments in diverse fields, ranging from biology to materials science. (c) Knowledge and skills. (1) The student will be able to write both common an IUPAC names for the hydrocarbon.
    [Show full text]
  • HISTORICAL ASPECTS of ORGANIC CHEMISTRY TEACHING (On the Example of Chemistry Direction of Higher Educational Institutions)
    Journal of Critical Reviews ISSN- 2394-5125 Vol 7, Issue 13, 2020 CONCEPTUAL - HISTORICAL ASPECTS OF ORGANIC CHEMISTRY TEACHING (on the example of chemistry direction of Higher educational institutions) Rajabov Khudayor Madrimovich Uzbekistan, Khorasm region, Rajabov Khudayor Madrimovich, Doctor of philosophy (PhD) on pedagogical sciences, Urganch State University E-mail: [email protected] Received: 16.04.2020 Revised: 18.05.2020 Accepted: 13.06.2020 Abstract. The article reveals the historical approach on the teaching of organic chemistry in pedagogical universities. The development of modern trends and general competencies of students on the basis of historical approach, the creation of educational motivation, the focus on independent research and training of creative specialists are the most important directions. In this regard, it is important to improve the technology for organizing the educational process on the basis of historical principles in the system of training future chemistry teachers, to improve the mechanisms on the methodological support, to fulfill the system of competencies and cyclic diagnostics. Keywords: historical approach, organic chemistry, conceptual - historical aspects, professional competence, principle of historicism, methodology, self-improvement, innovation, non-historical, positive attitude, extracurricular activities. © 2020 by Advance Scientific Research. This is an open-access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/) DOI: http://dx.doi.org/10.31838/jcr.07.13.129
    [Show full text]
  • Reactions of Alkenes and Alkynes
    05 Reactions of Alkenes and Alkynes Polyethylene is the most widely used plastic, making up items such as packing foam, plastic bottles, and plastic utensils (top: © Jon Larson/iStockphoto; middle: GNL Media/Digital Vision/Getty Images, Inc.; bottom: © Lakhesis/iStockphoto). Inset: A model of ethylene. KEY QUESTIONS 5.1 What Are the Characteristic Reactions of Alkenes? 5.8 How Can Alkynes Be Reduced to Alkenes and 5.2 What Is a Reaction Mechanism? Alkanes? 5.3 What Are the Mechanisms of Electrophilic Additions HOW TO to Alkenes? 5.1 How to Draw Mechanisms 5.4 What Are Carbocation Rearrangements? 5.5 What Is Hydroboration–Oxidation of an Alkene? CHEMICAL CONNECTIONS 5.6 How Can an Alkene Be Reduced to an Alkane? 5A Catalytic Cracking and the Importance of Alkenes 5.7 How Can an Acetylide Anion Be Used to Create a New Carbon–Carbon Bond? IN THIS CHAPTER, we begin our systematic study of organic reactions and their mecha- nisms. Reaction mechanisms are step-by-step descriptions of how reactions proceed and are one of the most important unifying concepts in organic chemistry. We use the reactions of alkenes as the vehicle to introduce this concept. 129 130 CHAPTER 5 Reactions of Alkenes and Alkynes 5.1 What Are the Characteristic Reactions of Alkenes? The most characteristic reaction of alkenes is addition to the carbon–carbon double bond in such a way that the pi bond is broken and, in its place, sigma bonds are formed to two new atoms or groups of atoms. Several examples of reactions at the carbon–carbon double bond are shown in Table 5.1, along with the descriptive name(s) associated with each.
    [Show full text]
  • Che 360: Polymer Chemistry Syllabus
    CHE 360: POLYMER CHEMISTRY SYLLABUS Instructor: Dr. Zachary Rodgers Text: Introduction to Polymer Chemistry (Carraher) Course webpage: Desire2Learn Prerequisites: CHE 262: Organic Chemistry Contact Info: (724)-946-6289 [email protected] Class Time: TR 9:10 – 10:50 am Lab Time: R 2:00 – 5:00 pm Course Overview The word polymer comes from the Greek words “poly”, meaning many, and “mer”, meaning parts. Like the macrostructures we see every day, such as a house built of brick, the larger structures of polymers have very different properties from their smaller chemical building blocks. The uniqueness of polymer properties provide most of the materials we interact with on a regular basis, including our clothes, plastics, paper, adhesives, and even our bodies themselves. Therefore, no education in chemistry would be complete without describing the general properties, synthesis, processing, and function of polymeric materials. This semester long course aims to: Describe how polymer morphology affects a polymer’s overall properties and behavior Teach polymer characterization techniques to determine their structure and size Detail a variety of polymerization mechanisms and their underlying kinetic/thermodynamic characteristics Introduce the practical techniques used to synthesize a wide range of polymeric structures Provide several examples of the industrial processing techniques used to generate consumable polymer products Make connections between material to answer complex and multi-step problems Expose students to literature research in materials and polymer science Grading Grading Weights 10% Homework Assignments (~6 – 8 total) 20% Laboratory Grade 37.5% Exams (3 Tests) 12.5% Student Presentation 20% Final Grading Scale 90 - 100 A 72 – 77 C 88 - 89 B+ 70 – 71 C- 82 – 87 B 68 – 69 D+ 80 – 81 B- 60 – 67 D 78 – 79 C+ < 60 F The scale set in this syllabus is non-negotiable.
    [Show full text]
  • Introduction to Theory of Chemical Reactions
    INTRODUCTION TO THEORY OF CHEMICAL REACTIONS BACKGROUND The introductory part of the organic chemistry course has three major modules: Molecular architecture (structure), molecular dynamics (conformational analysis), and molecular transformations (chemical reactions). An understanding of the first two is crucial to an understanding of the third one. The rest of the organic chemistry course will be largely spent on studying different kinds of reactions and mechanisms. A summary of key concepts follows. 1. MOLECULAR ARCHITECTURE - Basic principles of molecular structure. a) Atomic structure b) Orbitals and hybridization c) Covalent bonding d) Lewis structures and resonance forms e) Isomerism, structural and geometric isomers f) Polarity, functional groups, nomenclature systems g) Three-dimensional structures, stereochemistry, stereoisomers. 2. MOLECULAR DYNAMICS - Basic principles of molecular motion involving rotation around single bonds and no bond breakage. The focus is on conformations and their energy relationships, especially in reference to alkanes and cycloalkanes (conformational analysis). a) Steric interactions b) Torsional strain and Newman projections c) Angle strain in cycloalkanes d) Conformations of cyclohexane and terminology associated with it. 3. MOLECULAR TRANSFORMATIONS - This is the part that comprises the bulk of organic chemistry courses. It is the study of chemical reactions and the principles that rule transformations. There are three major aspects of this module. In organic chemistry I we will focus largely on the first two, and leave the study of synthetic strategy for later. a) Reaction mechanisms - Step by step accounts of how electron movement takes place when bonds are broken and formed, and the conditions that favor these processes (driving forces). An understanding of the basic concepts of thermodynamics and kinetics is important here.
    [Show full text]
  • Organic Chemistry I: Reactions and Overview
    Organic Chemistry I: Reactions and Overview Andrew Rosen Editor: Raghav Malik January 13, 2013 Contents I Library of Synthetic Reactions 3 II Organic Trends and Essentials 4 1 The Basics: Bonding and Molecular Structure 4 1.1 Resonance Stability . 4 2 Families of Carbon Compounds 4 2.1 Strength of London Dispersion Forces (Polarizability) . 4 2.2 Degree of Unsaturation . 4 3 An Introduction to Organic Reactions and Their Mechanisms 4 3.1 Comparing Acid Strengths . 4 4 Nomenclature and Conformations of Alkanes and Cycloalkanes 5 4.1 Ring Flipping . 5 5 Stereochemistry 5 5.1 Naming Enantiomers via the -R and -S System . 5 5.2 Stereochemistry Examples . 6 6 Ionic Reactions - Overview 6 6.1 General Nucleophilic Substitution Reactions . 6 6.2 Carbocation Stability . 6 6.3 Factors Aecting the Rates of SN 1 and SN 2 Reactions . 6 6.4 Elimination Reactions . 7 6.5 Summary . 7 7 Alkenes and Alkynes I - Overview 8 7.1 The E-Z System . 8 7.2 Relative Stabilities of Alkenes . 8 7.3 Factors Aecting Elimination Reactions . 8 7.4 Acid-Catalyzed Dehydration of Alcohols . 8 1 III Reaction Mechanisms 9 8 Ionic Reactions - Mechanisms 9 8.1 The SN 2 Reaction . 9 8.2 The SN 1 Reaction . 10 8.3 The E2 Reaction . 10 8.4 The E1 Reaction . 11 9 Alkenes and Alkynes I - Mechanisms 11 9.1 Acid-Catalyzed Dehydration of Secondary or Tertiary Alcohols: An E1 Reaction . 11 9.2 Acid-Catalyzed Dehydration of Primary Alcohols: An E2 Reaction . 12 9.3 Synthesis of Alkynes from Vic-Dihalides .
    [Show full text]
  • Introduction to Biology. Lecture 6
    Where we are? Origin of life Introduction to Biology. Lecture 6 Alexey Shipunov Minot State University September 5, 2012 Shipunov Introduction to Biology. Lecture 6 Where we are? Origin of life Outline 1 Where we are? 2 Origin of life Molecules of life Primordial living structures Alternatives and amendments to abiogenesis Shipunov Introduction to Biology. Lecture 6 Where we are? Origin of life Outline 1 Where we are? 2 Origin of life Molecules of life Primordial living structures Alternatives and amendments to abiogenesis Shipunov Introduction to Biology. Lecture 6 Where we are? Origin of life Evolution is the fact and research program Given the amount of evidence presented, evolution is a fact Evolution is also an extremely useful, working research program, both in biology and medicine Shipunov Introduction to Biology. Lecture 6 Molecules of life Where we are? Primordial living structures Origin of life Alternatives and amendments to abiogenesis Origin of life Molecules of life Shipunov Introduction to Biology. Lecture 6 Molecules of life Where we are? Primordial living structures Origin of life Alternatives and amendments to abiogenesis Organic chemistry: chemistry of carbon Carbon skeleton And H, O, N, P, S Shipunov Introduction to Biology. Lecture 6 Molecules of life Where we are? Primordial living structures Origin of life Alternatives and amendments to abiogenesis Four types of biomolecules Lipids: hydrophobic Carbohydrates (sugars): multiple −OH groups Amino acids: N + C + O and hydrogen Nucleotides: cycle with nitrogen (heterocycle), sugar and phosphoric acid Shipunov Introduction to Biology. Lecture 6 Molecules of life Where we are? Primordial living structures Origin of life Alternatives and amendments to abiogenesis Organic polymers Polymeric carbohydrates: polysaccharides (like cellulose and starch) Polymeric amino acids: proteins Polymeric nucleotides: nucleic acids (DNA and RNA) Shipunov Introduction to Biology.
    [Show full text]
  • Chapter 1 Organic Molecules and Chemical Bonding
    (4,5,9,11,12/98)(1,9,10/99) Neuman Chapter 1 Chapter 1 Organic Molecules and Chemical Bonding from Organic Chemistry by Robert C. Neuman, Jr. Professor of Chemistry, emeritus University of California, Riverside [email protected] <http://web.chem.ucsb.edu/~neuman/orgchembyneuman/> Chapter Outline of the Book ************************************************************************************** I. Foundations 1. Organic Molecules and Chemical Bonding 2. Alkanes and Cycloalkanes 3. Haloalkanes, Alcohols, Ethers, and Amines 4. Stereochemistry 5. Organic Spectrometry II. Reactions, Mechanisms, Multiple Bonds 6. Organic Reactions *(Not yet Posted) 7. Reactions of Haloalkanes, Alcohols, and Amines. Nucleophilic Substitution 8. Alkenes and Alkynes 9. Formation of Alkenes and Alkynes. Elimination Reactions 10. Alkenes and Alkynes. Addition Reactions 11. Free Radical Addition and Substitution Reactions III. Conjugation, Electronic Effects, Carbonyl Groups 12. Conjugated and Aromatic Molecules 13. Carbonyl Compounds. Ketones, Aldehydes, and Carboxylic Acids 14. Substituent Effects 15. Carbonyl Compounds. Esters, Amides, and Related Molecules IV. Carbonyl and Pericyclic Reactions and Mechanisms 16. Carbonyl Compounds. Addition and Substitution Reactions 17. Oxidation and Reduction Reactions 18. Reactions of Enolate Ions and Enols 19. Cyclization and Pericyclic Reactions *(Not yet Posted) V. Bioorganic Compounds 20. Carbohydrates 21. Lipids 22. Peptides, Proteins, and α−Amino Acids 23. Nucleic Acids **************************************************************************************
    [Show full text]
  • Organic Chemistry to Biochemistry
    page 1 Metabolisn1 Review: Step by Step from Organic Chemistry to Biochemistry Overview: This handout contains a review of the fundamental parts of organic chemistry needed for metabolism. Dr. Richard Feinman Department of Biochemistry Room 7-20, BSB (718) 270-2252 [email protected] STEP-BY-STEP: ORGANIC CHEMISTRY TO NUTRITION AND METABOLISM page 2 CHAPTER O. INTRODUCTION Where we're going. The big picture in nutrition and metabolism is shown in a block diagram or "black box" diagram. A black box approach shows inputs and outputs to a process that may not be understood. It is favored by engineers who are the group that are most uncomfortable with the idea that they don't know anything at all. The black box approach can frequently give ----c02 you some insight because it organizes whatever you do know. For example: ENERGY CELL MA TERIA L 1. Even though the block diagram is very simple, just looking at the inputs and outputs gives us some useful information. il The diagram says animals obtain energy by the oxidation of food to CO2 and water. Although you knew this before, the diagram highlights the fact that understanding biochemistry probably involves understanding oxidation-reduction reactions. 2. The diagram also indicates what might not be obvious: a major part of the energy obtained from oxidation of food is used to make new cell material. Although we think of organisms using energy for locomotion or to do physical work, in fact, most of the energy used is chemical energy. 3. Inside the black boxes in the diagram contain are the (organic) chemical reactions that convert food into energy and cell material.
    [Show full text]
  • Chemistry & Biochemistry
    Chemistry & Biochemistry 1 Chemistry & Biochemistry BS curriculum in Chemistry and BS curriculum in Biochemistry These curricula, approved by the American Chemical Society, prepare students for careers in pure and applied chemistry with a dual emphasis on classroom and laboratory experience. A flexible senior year allows student to tailor the program to individual professional goals. Graduates are prepared to enter the profession immediately or continue for advanced degree programs. The senior research program introduces students to modern advanced techniques and approaches to chemical research in an area of their interest by having them complete an individual research project in conjunction with a faculty adviser. BA curriculum in Chemistry The BA curriculum in Chemistry provides a strong background in chemistry while allowing students to specialize in areas of interest. It is especially well suited for students leaning towards medical sciences while allowing more flexibility than that allowed in the American Chemical Society approved biochemistry curriculum. The program allows for great versatility in the junior and senior years, allowing the curriculum to be tailored to individual goals. The curriculum prepares students for professional careers in chemistry or biochemistry and advanced degree programs in chemistry, biochemistry and medically related fields. Clinical Laboratory Sciences The Division of Clinical Laboratory Sciences has two curricula leading to the degree of bachelor of science in laboratory technology or bachelor of science in medical technology. These curricula prepare students for medical laboratory careers in fields such as public health, bacteriology, environmental testing, industrial quality control, research and forensic science. Graduates may choose to qualify as certified medical technologists, which is accomplished by successfully completing a 12-month training period (rotating hospital internship) in an accredited school of medical technology and passing a national certifying examination.
    [Show full text]
  • Physical Organic Chemistry
    Physical organic chemistry Edited by John Murphy Generated on 24 September 2021, 10:07 Imprint Beilstein Journal of Organic Chemistry www.bjoc.org ISSN 1860-5397 Email: [email protected] The Beilstein Journal of Organic Chemistry is published by the Beilstein-Institut zur Förderung der Chemischen Wissenschaften. This thematic issue, published in the Beilstein Beilstein-Institut zur Förderung der Journal of Organic Chemistry, is copyright the Chemischen Wissenschaften Beilstein-Institut zur Förderung der Chemischen Trakehner Straße 7–9 Wissenschaften. The copyright of the individual 60487 Frankfurt am Main articles in this document is the property of their Germany respective authors, subject to a Creative www.beilstein-institut.de Commons Attribution (CC-BY) license. Physical organic chemistry John A. Murphy Editorial Open Access Address: Beilstein J. Org. Chem. 2010, 6, 1025. WestCHEM, Department of Pure and Applied Chemistry, University of doi:10.3762/bjoc.6.116 Strathclyde, 295 Cathedral Street, Glasgow G1 1XL, U.K Received: 01 November 2010 Email: Accepted: 01 November 2010 John A. Murphy - [email protected] Published: 03 November 2010 Guest Editor: J. Murphy © 2010 Murphy; licensee Beilstein-Institut. License and terms: see end of document. Physical organic chemistry – the study of the interplay between I am privileged to act as Guest Editor for this Thematic Series structure and reactivity in organic molecules – underpins of the Beilstein Journal of Organic Chemistry, and hope that organic chemistry, and we cannot imagine organic chemistry as you enjoy the papers that form this issue. I am grateful to the a subject without knowledge of mechanism and reactivity.
    [Show full text]