1
answer
0
watching
336
views
11 Dec 2019
Section 12.3 APPLICATIONS OF DIELS-ALDER REACTIONS. PART A. REACTION OF 1,3-BUTADIENE AND MALEIC ANHYDRIDE
4. Why is 3-sulfolene rather than 1,3-butadiene itself to be used as a source of the diene?
7. What is the limiting reagent in the reaction between 1,3-butadiene and maleic anhydride and why do you think this reagent rather than the other was made limiting? Show your calculations.
10. Is either 3-sulfolene or maleic anhydride mutagenic?
11. The flash point (°C) of xylene is .
12. List the possible effects of inhaling excessive amounts of xylene.
Section 12.3 APPLICATIONS OF DIELS-ALDER REACTIONS. PART A. REACTION OF 1,3-BUTADIENE AND MALEIC ANHYDRIDE
4. Why is 3-sulfolene rather than 1,3-butadiene itself to be used as a source of the diene?
7. What is the limiting reagent in the reaction between 1,3-butadiene and maleic anhydride and why do you think this reagent rather than the other was made limiting? Show your calculations.
10. Is either 3-sulfolene or maleic anhydride mutagenic?
11. The flash point (°C) of xylene is .
12. List the possible effects of inhaling excessive amounts of xylene.
Casey DurganLv2
13 Dec 2019
Related textbook solutions
Basic Chemistry
5 Edition,
Timberlake
ISBN: 9780134138046
Principles of Chemistry Molecular Approach
4th Edition,
Tro
ISBN: 9780134112831
Principles of Chemistry Molecular Approach
3rd Edition, 2014
Tro
ISBN: 9780321971944
Chemistry: Structure and Properties
2nd Edition,
Tro
ISBN: 9780134293936
Chemistry: A Molecular Approach
3rd Edition,
Tro
ISBN: 9780321809247
Chemistry: A Molecular Approach
5th Edition,
Tro
ISBN: 9780134874371
Principles of Chemistry: A Molecular Approach
4th Edition,
Tro
ISBN: 9780134895741
Chemistry: The Central Science
14th Edition, 2017
Brown
ISBN: 9780134414232