Organic Chemistry Concepts An EFL Approach
Auteurs : Roos Gregory, Roos Cathryn
Organic Chemistry Concepts: An EFL Approach provides an introductory overview of the subject, to enable the reader to understand many critical, experimental facts. Designed to cover a single-semester course or a needed review on the principles of Organic Chemistry, the book is written and organized for readers whose first language is not English. Approximately 80% of the words used are drawn from the list of the 2,000 most common English words; the remaining 20% includes necessary technical words, common chemistry terms, and well-known academic words (per the Academic Word List). The book has been class-tested internationally as well as with native English speakers, and differs from other introductory textbooks in the subject both in its coverage and organization, with a particular focus on common problem areas. Focused on a limited number of functional classes, Organic Chemistry Concepts: An EFL Approach introduces those organic compounds early in the book. Once readers have a foundation of the concepts and language of organic chemistry, they can build from that knowledge and work with relatively complex molecules, such as some natural product types covered in a later chapter. The book describes basic level reaction mechanisms when instructive, and illustrations throughout to emphasize the 3D nature of organic chemistry. The book includes multiple pedagogical features, such as chapter questions and useful appendices, to support reader comprehension.
Organic chemistry lecturers supporting non-native English speaking students, and these students themselves
His research interests have focused on the development of synthetic methodology, with particular interest in asymmetric processes. This provided numerous publications in the areas of the Baylis-Hillman reaction, imidazolidinone chiral auxiliaries, and dirhodium catalyst development and applications. This period also included a number of productive collaborative visits with Tony McKervey (University College Cork & Queen’s University, Belfast), C. K. Sha (Shin Hua University, Taiwan), Mike Doyle (Trinity University, San Antonio), and Ron Warrener (CQU Rockhampton, Queensland). In 2001 he received the Merck Gold Medal for research from the South African Chemical Institute.
Cathryn Roos holds a Master's degree in Curriculum from the University of Toronto, a Certificate of TESL from Carleton University, and an undergraduate degree in Anthropology at the University of Manitoba. She is currently an English language instructor at Zayed University in Dubai, United Arab Emirates. Previously, she worked at the Petroleum Institute in Abu Dhabi, Sultan Qaboos University in Oman, and the Toronto Board of Education in Canada. She has also taught in Japan and Nigeria. Throughout her care
- Covers all primary concepts in accessible language and pedagogical features, worked examples, glossary, chapter questions, illustrations, and useful summaries
- Builds a foundation of key material through a structured framework from which readers can expand their understanding
- Contains class-tested content written in a straightforward and accessible manner for non-native English speakers
Date de parution : 10-2014
Ouvrage de 236 p.
19x23.3 cm
Thème d’Organic Chemistry Concepts :
Mots-clés :
3-D drawings; Acetal; Acidity; Acylation; Addition; Aldose; Alkylation; Amino acid; Basicity; Biomolecule; Brønsted-Lowry; Carbanion; Carbocation; Carbohydrate; Carbon bonding; Carbon oxidation states; Cis-trans; Combustion; Compound class; Condensation; Configuration; Conformational isomers; Conjugate base; Conjugation; Curly arrows; Dehydration; Delocalization; Diagnostic test; Electron acceptor; Electron donor; Electronic effects; Electrophile; Electrophilic addition; Electrophilic aromatic substitution; Elimination; Enantiomer; Energy diagram; Enolate; Epoxidation; Fatty acid; Free radical substitution; Functional group; Geometric isomers; Glyceride; Grignard; Haloform; Halogenation; Heterolysis; Homolysis; Hybrid structure; Hybridization model molecular shape; Hydrate; Hydration; Hydrogenation; Hydroxylation; Inductive effect; Intermediate; Intermolecular forces; Ketose; Lewis; Lipid; Markovnikov; Mechanism; Metal hydride; Molecular diagrams; Molecular isomers; Natural product; Nucleic acid; Nucleophile; Nucleophilic acyl substitution; Nucleophilic substitution; Oils; Optical isomers; Organometallic; Oxidation; Ozonolysis; Peptide; Physical properties; Polarity; Protein; Proton; Radicals; Rearrangement; Reduction; Resonance; Stability; Steroid; Structural isomers; Substitution; Systematic compound naming; Tautomer; Transition state; Waxes; Zwitterion