ZP282 - Organic chemistry II
Course specification | ||||
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Course title | Organic chemistry II | |||
Acronym | ZP282 | |||
Study programme | Biochemical Engineering and Biotechnology,Chemical Engineering | |||
Module | ||||
Lecturer (for classes) | ||||
Lecturer/Associate (for practice) | ||||
Lecturer/Associate (for OTC) | ||||
ESPB | 7.0 | Status | ||
Condition | Organic chemistry I | Облик условљености | ||
The goal | Introduction to the basic concepts of the structure and reactions of organic compounds, the nomenclature of organic compounds, dependence of the physical and chemical properties and molecular structure, the possibilities of synthesis of organic molecules and their application. Correlation between the structure and reactivity of organic molecules and its application. | |||
The outcome | Students will acquire basic theoretical knowledge of organic chemistry and together with the gained laboratory skills it will allow them to solve problems of the synthesis and reactivity of organic molecules. | |||
Contents | ||||
Contents of lectures | Amines and their derivatives: synthesis and properties. Correlation between the structure and basicity of amines. Diazotization and diazo coupling reactions. Application in the synthesis. Nitro compounds: structure and properties. Aromatic nitro compounds, explosives. Aldehydes and ketones: structure, properties and synthesis. Nucleophilic addition to carbonyl group. Enolates and enols. Keto-enol equilibrium. Aldol reaction. Properties of α, β-unsaturated aldehydes and ketones and the conjugate addition reactions. Carboxylic acids: structure, properties and synthesis. Correlation between the structure and acidity. Reactions of carboxylic acids. Conversion to derivatives. Nucleophilic acyl substitution. α-Halogen substituted acids and their reactions. Carboxylic acids derivatives: acyl-halides, anhydrides, esters, amides and nitriles. The structure, properties, synthesis and reactivity in nucleophilic acyl substitution reaction. Synthesis and reactions of β-dikarbonilnih compounds. Ester enolates and Claisen condensation. Malonic ester and acetoacetic ester synthesis. Strategy of synthesis. Carbohydrates: polyfunctional natural compounds. Lipids. Heterocyclic aromatic compounds: structure and properties. Five- and six-member rings. Synthesis and characteristic reactions. Condensed ring systems. Amino acids, proteins and nucleic acids. | |||
Contents of exercises | Synthesis of 6 organic compounds that illustrate the most important organic reactions. | |||
Literature | ||||
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Number of hours per week during the semester/trimester/year | ||||
Lectures | Exercises | OTC | Study and Research | Other classes |
4 | 0 | 2 | ||
Methods of teaching | Lectures, Organic Chemistry Laboratory, Written mid-term exams. | |||
Knowledge score (maximum points 100) | ||||
Pre obligations | Points | Final exam | Points | |
Activites during lectures | 5 | Test paper | 50 | |
Practical lessons | 15 | Oral examination | ||
Projects | ||||
Colloquia | 30 | |||
Seminars |