Patrick E. McMahon has for the past twenty three years been teaching both general chemistry and organic chemistry at Benedictine University in Lisle, Illinois. Prior to that, he was a research scientist for Amoco Chemical Company at the Naperville, Illinois campus. McMahon has also taught at several institutions in the Chicago area, including Elmhurst College, Dominican University and Triton Community College. He is a member of the American Legion and served in the United States Army from 1970-1972. His main area of research interest is organic reaction catalysis. Awards that can be accredited to his name include the B.J. Babler award for outstanding contribution to under-graduate instruction at the University of Illinois, the Dean’s Award for Teaching Excellence at Benedictine University and first recipient of the Shining Star award given by the student senate for outstanding contribution to students at Benedictine University.Bohdan B. Khomtchouk is a triple-major summa cum laude (B.Sc. Biochemistry and Molecular Biology, B.Sc. Mathematics and B.Sc. Physics) and is currently United States Department of Defense NDSEG Fellow at the University of Miami Miller School of Medicine.Claes Wahlestedt, MD, PhD, is Leonard M. Miller Professor at the University of Miami Miller School of Medicine and is working on a range of chemistry related translational efforts in his roles as Associate Dean and Center Director for Therapeutic Innovation. The author of some 250 peer reviewed scientific publications with 30,000+ citations, his ongoing research projects concern chemical biology, epigenetics, genomics and drug/biomarker discovery across several therapeutic areas. He has experience not only from academia, but also from leadership positions in the pharmaceutical industry, namely Astra-Zeneca, Pharmacia & Upjohn and Pharmacia Corporation.

'In Survival Guide to Organic Chemistry, the authors approach concepts in organic chemistry from an angle that differs from most textbooks. Rather than the usual approach of heavy paragraphs and figures, they establish a process wherein each concept is broken into a series of manageable steps, each of which involves a singular aspect of an overarching theme. Each step includes an example illustrating that singular process. This method allows students to approach material at levels within their control, rather than all at once for any given concept. The text also provides a framework for organizing reactions and includes over 30 practice exams spanning concepts of both semesters of a typical undergraduate organic chemistry sequence. In addition to students entering organic chemistry, this text could also serve as a useful reference for students in upper-level undergraduate or graduate level courses who need to refresh fundamental concepts before delving into more complex material. Finally, faculty may find this useful as a source of practice problems in class, as well as a means of guiding conversations for students struggling with particular concepts.--J. Tedesco, Lake Erie CollegeSumming Up: Recommended. Lower-division undergraduates and above; faculty and professionals.'– J. Tedesco, for CHOICE, January 2018, Vol. 55, No. 5.

• Chapter 1: General Concepts for Covalent Bonding and Constructing Lewis Structures for Organic Molecules. Chapter 2: Guideline for Writing Organic Molecule Isomers and Determining Number of Rings Plus Pi-Bonds. Chapter 3: Guideline for Complete Analysis for Central Atoms and Molecules: Bonding/Hybridization/Geometry/Polarity. Chapter 4: Notation in Organic Chemistry: Guide to Writing and Using Condensed Formulas and Line Drawings. Chapter 5: Summary Guidelines for Organic Nomenclature. Chapter 6: Guidelines for Analysis of Intermolecular Forces for Organic Molecules. Chapter 7: Alkane and Cycloalkane Conformations. Chapter 8: Summary Guide to Thermodynamic Concepts for Organic Chemistry. Chapter 9: Guide to Kinetics and Reaction Mechanisms. Chapter 10: Review of Acid/Base Concepts for Organic Chemistry. Chapter 11: Electrophiles and Nucleophiles in Organic Reaction Mechanisms. Chapter 12: Conceptual Guide to Mechanisms in Organic Chemistry. Chapter 13: Guide to Stereochemistry Concepts and Analysis of Reaction Stereochemistry as Applied to Electrophilic Addition. Chapter 14: A Process for Calculation of Product Distribution Through Relative Rate Analysis: Examples for Free Radical Halogenation. Chapter 15: Process to Identify and Solve the Reactions for Organic I. Chapter 16: Electrophilic Addition and Addition/Elimination to Conjugated Double Bond and Aromatic Systems. Chapter 17: Oxidation/Reduction Relationships for Carbonyl Carbon. Chapter 18: A Complete System for Organizing, Identifying, and Solving Carbonyl Reactions: Nucleophilic Addition and Addition/Elimination. Chapter 19: A Brief Guideline for Applying Fundamental Concepts in NMR Spectroscopy. Organic I Practice Exams. Organic II Practice Exams. Multiple Choice Exams.

Patrick E. McMahon has for the past twenty three years been teaching both general chemistry and organic chemistry at Benedictine University in Lisle, Illinois. Prior to that, he was a research scientist for Amoco Chemical Company at the Naperville, Illinois campus. McMahon has also taught at several institutions in the Chicago area, including Elmhurst College, Dominican University and Triton Community College. He is a member of the American Legion and served in the United States Army from 1970-1972. His main area of research interest is organic reaction catalysis. Awards that can be accredited to his name include the B.J. Babler award for outstanding contribution to under-graduate instruction at the University of Illinois, the Dean’s Award for Teaching Excellence at Benedictine University and first recipient of the Shining Star award given by the student senate for outstanding contribution to students at Benedictine University.Bohdan B. Khomtchouk is a triple-major summa cum laude (B.Sc. Biochemistry and Molecular Biology, B.Sc. Mathematics and B.Sc. Physics) and is currently United States Department of Defense NDSEG Fellow at the University of Miami Miller School of Medicine.Claes Wahlestedt, MD, PhD, is Leonard M. Miller Professor at the University of Miami Miller School of Medicine and is working on a range of chemistry related translational efforts in his roles as Associate Dean and Center Director for Therapeutic Innovation. The author of some 250 peer reviewed scientific publications with 30,000+ citations, his ongoing research projects concern chemical biology, epigenetics, genomics and drug/biomarker discovery across several therapeutic areas. He has experience not only from academia, but also from leadership positions in the pharmaceutical industry, namely Astra-Zeneca, Pharmacia & Upjohn and Pharmacia Corporation.

'In Survival Guide to Organic Chemistry, the authors approach concepts in organic chemistry from an angle that differs from most textbooks. Rather than the usual approach of heavy paragraphs and figures, they establish a process wherein each concept is broken into a series of manageable steps, each of which involves a singular aspect of an overarching theme. Each step includes an example illustrating that singular process. This method allows students to approach material at levels within their control, rather than all at once for any given concept. The text also provides a framework for organizing reactions and includes over 30 practice exams spanning concepts of both semesters of a typical undergraduate organic chemistry sequence. In addition to students entering organic chemistry, this text could also serve as a useful reference for students in upper-level undergraduate or graduate level courses who need to refresh fundamental concepts before delving into more complex material. Finally, faculty may find this useful as a source of practice problems in class, as well as a means of guiding conversations for students struggling with particular concepts.--J. Tedesco, Lake Erie CollegeSumming Up: Recommended. Lower-division undergraduates and above; faculty and professionals.'– J. Tedesco, for CHOICE, January 2018, Vol. 55, No. 5.

• Chapter 1: General Concepts for Covalent Bonding and Constructing Lewis Structures for Organic Molecules. Chapter 2: Guideline for Writing Organic Molecule Isomers and Determining Number of Rings Plus Pi-Bonds. Chapter 3: Guideline for Complete Analysis for Central Atoms and Molecules: Bonding/Hybridization/Geometry/Polarity. Chapter 4: Notation in Organic Chemistry: Guide to Writing and Using Condensed Formulas and Line Drawings. Chapter 5: Summary Guidelines for Organic Nomenclature. Chapter 6: Guidelines for Analysis of Intermolecular Forces for Organic Molecules. Chapter 7: Alkane and Cycloalkane Conformations. Chapter 8: Summary Guide to Thermodynamic Concepts for Organic Chemistry. Chapter 9: Guide to Kinetics and Reaction Mechanisms. Chapter 10: Review of Acid/Base Concepts for Organic Chemistry. Chapter 11: Electrophiles and Nucleophiles in Organic Reaction Mechanisms. Chapter 12: Conceptual Guide to Mechanisms in Organic Chemistry. Chapter 13: Guide to Stereochemistry Concepts and Analysis of Reaction Stereochemistry as Applied to Electrophilic Addition. Chapter 14: A Process for Calculation of Product Distribution Through Relative Rate Analysis: Examples for Free Radical Halogenation. Chapter 15: Process to Identify and Solve the Reactions for Organic I. Chapter 16: Electrophilic Addition and Addition/Elimination to Conjugated Double Bond and Aromatic Systems. Chapter 17: Oxidation/Reduction Relationships for Carbonyl Carbon. Chapter 18: A Complete System for Organizing, Identifying, and Solving Carbonyl Reactions: Nucleophilic Addition and Addition/Elimination. Chapter 19: A Brief Guideline for Applying Fundamental Concepts in NMR Spectroscopy. Organic I Practice Exams. Organic II Practice Exams. Multiple Choice Exams.

Patrick E. McMahon has for the past twenty three years been teaching both general chemistry and organic chemistry at Benedictine University in Lisle, Illinois. Prior to that, he was a research scientist for Amoco Chemical Company at the Naperville, Illinois campus. McMahon has also taught at several institutions in the Chicago area, including Elmhurst College, Dominican University and Triton Community College. He is a member of the American Legion and served in the United States Army from 1970-1972. His main area of research interest is organic reaction catalysis. Awards that can be accredited to his name include the B.J. Babler award for outstanding contribution to under-graduate instruction at the University of Illinois, the Dean’s Award for Teaching Excellence at Benedictine University and first recipient of the Shining Star award given by the student senate for outstanding contribution to students at Benedictine University.Bohdan B. Khomtchouk is a triple-major summa cum laude (B.Sc. Biochemistry and Molecular Biology, B.Sc. Mathematics and B.Sc. Physics) and is currently United States Department of Defense NDSEG Fellow at the University of Miami Miller School of Medicine.Claes Wahlestedt, MD, PhD, is Leonard M. Miller Professor at the University of Miami Miller School of Medicine and is working on a range of chemistry related translational efforts in his roles as Associate Dean and Center Director for Therapeutic Innovation. The author of some 250 peer reviewed scientific publications with 30,000+ citations, his ongoing research projects concern chemical biology, epigenetics, genomics and drug/biomarker discovery across several therapeutic areas. He has experience not only from academia, but also from leadership positions in the pharmaceutical industry, namely Astra-Zeneca, Pharmacia & Upjohn and Pharmacia Corporation.

'In Survival Guide to Organic Chemistry, the authors approach concepts in organic chemistry from an angle that differs from most textbooks. Rather than the usual approach of heavy paragraphs and figures, they establish a process wherein each concept is broken into a series of manageable steps, each of which involves a singular aspect of an overarching theme. Each step includes an example illustrating that singular process. This method allows students to approach material at levels within their control, rather than all at once for any given concept. The text also provides a framework for organizing reactions and includes over 30 practice exams spanning concepts of both semesters of a typical undergraduate organic chemistry sequence. In addition to students entering organic chemistry, this text could also serve as a useful reference for students in upper-level undergraduate or graduate level courses who need to refresh fundamental concepts before delving into more complex material. Finally, faculty may find this useful as a source of practice problems in class, as well as a means of guiding conversations for students struggling with particular concepts.--J. Tedesco, Lake Erie CollegeSumming Up: Recommended. Lower-division undergraduates and above; faculty and professionals.'– J. Tedesco, for CHOICE, January 2018, Vol. 55, No. 5.

• Chapter 1: General Concepts for Covalent Bonding and Constructing Lewis Structures for Organic Molecules. Chapter 2: Guideline for Writing Organic Molecule Isomers and Determining Number of Rings Plus Pi-Bonds. Chapter 3: Guideline for Complete Analysis for Central Atoms and Molecules: Bonding/Hybridization/Geometry/Polarity. Chapter 4: Notation in Organic Chemistry: Guide to Writing and Using Condensed Formulas and Line Drawings. Chapter 5: Summary Guidelines for Organic Nomenclature. Chapter 6: Guidelines for Analysis of Intermolecular Forces for Organic Molecules. Chapter 7: Alkane and Cycloalkane Conformations. Chapter 8: Summary Guide to Thermodynamic Concepts for Organic Chemistry. Chapter 9: Guide to Kinetics and Reaction Mechanisms. Chapter 10: Review of Acid/Base Concepts for Organic Chemistry. Chapter 11: Electrophiles and Nucleophiles in Organic Reaction Mechanisms. Chapter 12: Conceptual Guide to Mechanisms in Organic Chemistry. Chapter 13: Guide to Stereochemistry Concepts and Analysis of Reaction Stereochemistry as Applied to Electrophilic Addition. Chapter 14: A Process for Calculation of Product Distribution Through Relative Rate Analysis: Examples for Free Radical Halogenation. Chapter 15: Process to Identify and Solve the Reactions for Organic I. Chapter 16: Electrophilic Addition and Addition/Elimination to Conjugated Double Bond and Aromatic Systems. Chapter 17: Oxidation/Reduction Relationships for Carbonyl Carbon. Chapter 18: A Complete System for Organizing, Identifying, and Solving Carbonyl Reactions: Nucleophilic Addition and Addition/Elimination. Chapter 19: A Brief Guideline for Applying Fundamental Concepts in NMR Spectroscopy. Organic I Practice Exams. Organic II Practice Exams. Multiple Choice Exams.