Advanced Organic Chemistry: verschil tussen versies
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[[Categorie:Machemie]] | [[Categorie:Machemie]] | ||
===21 januari 2019 VM=== | |||
====Examen==== | |||
[[Bestand:ExamAdvOrg21jan2019.png|800px]] | |||
====Oplossingen==== | |||
[[Media:SolutionsAdvOrg21jan2019jpg.jpg]] | |||
===28 januari 2013 NM=== | |||
[[Media:Examen organische chemie 23-01-2017.jpeg]] | [[Media:Examen organische chemie 23-01-2017.jpeg]] | ||
#Explain the following reaction. [[Bestand:org1.png]] | #Explain the following reaction. [[Bestand:org1.png]] | ||
#How is given cyclopropane synthesized from diethyl malonate in several steps? Choose reagents such that a maximal yield is obtained. [[Bestand:org2.png]] | #How is given cyclopropane synthesized from diethyl malonate in several steps? Choose reagents such that a maximal yield is obtained. [[Bestand:org2.png]] | ||
Versie van 22 jan 2019 13:57
Examenvragen
21 januari 2019 VM
Examen
Oplossingen
Media:SolutionsAdvOrg21jan2019jpg.jpg
28 januari 2013 NM
Media:Examen organische chemie 23-01-2017.jpeg
- Explain the following reaction.

- How is given cyclopropane synthesized from diethyl malonate in several steps? Choose reagents such that a maximal yield is obtained.

- This reaction scheme is an example of a benzannelation reaction. Upon heating, several consecutive steps happen so that the given end product is obtained. Among these steps are three electrocyclic reactions (two 4-electron and one 6-electron), a tautomerization, and a cycloaddition (not necessarily in this order).

- Explain formation of this product in presence of base.

- Give product A and explain how this reaction occurs.

- What products will be formed in following reactions?
