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  1. Courses

506389 - TRAINSHEEP - 2

courses
ID:
506389
Duration (hours):
36
CFU:
3
SSD:
Indefinito/Interdisciplinare
Year:
2025
  • Overview
  • Syllabus
  • Degrees

Overview

Date/time interval

Secondo Semestre (02/03/2026 - 12/06/2026)

Syllabus

Course Objectives

The course aims to deepen the experimental aspect of Organic Chemistry, completing the basic knowledge acquired previously with regard to the synthesis of organic molecules and experimental techniques.

Course Prerequisites

Having attended the Laboratory of Organic Chemistry

Teaching Methods

The course uses lectures for the explanation of experiences, followed by laboratory activities

Assessment Methods

The test consists of an oral exam that will focus on the experiences made in the laboratory and on the reports written by the student previously delivered

Texts

Vogel Chimica Organica Pratica Casa Editrice Ambrosiana - Milano
D.L. Pavia, G.M. Lampman, G. S. Kriz Il Laboratorio di Chimica Organica Ed. Sorbona – Milano
M. D’Ischia La Chimica Organica in Laboratorio Ed. Piccin

Contents

This objective will be achieved through laboratory experiences that use synthetic reactions learned in theoretical courses. The student will be directed to the evaluation of all aspects of a synthesis (optimization of yields, analysis of products with modern experimental techniques, safety of operations, etc.). Moreover it will explained how access to bibliographic information trough chemical databases

Here is reported the list of lab experiments:
• Preparation of ethyl (E)-4-methoxy-cinnamate-esters by Horner–Wadsworth–Emmons reaction between 4-methoxy-benzaldeyde and trimethyl phosphoacetate in aqueous solvent
• Reduction of Camphor to Borneol using Sodium Borohydride or Sodium metal
• Nifedipine synthesis through Hantzsch reaction.
• Photochemical reaction of Nifedipine monitored by HPLC analysis.
• Aldol reaction between 2-acetylpiridine and 4-nitrobenzaldehyde
• Synthesis of triphenylcarbinol by Grignard reaction between phenyl magnesium bromide and methyl benzoate.
• Friedel-Crafts acylation of methylbenzene
• Nitration of bromobenzene
The reactions are monitored by TLC and the products are characterized by spectroscopic IR, NMR or UV-Vis analysis.

Course Language

Italian

Degrees

Degrees

Chemistry 
Bachelor’s Degree
3 years
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