Antiaromatic - Study guides, Class notes & Summaries
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Exam (elaborations) TEST BANK FOR The Art of Writing Reasonable Organic Reaction Mechanisms 3rd Edition By Grossman
- Exam (elaborations) • 237 pages • 2021
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Exam (elaborations) TEST BANK FOR The Art of Writing Reasonable Organic Reaction Mechanisms 3rd Edition By Robert B. Grossman (Solution Manual) 
sp2 hybridization. One of the lone pairs is in a p orbital, and the other is in an sp2 orbital. Only 
the lone pair in the p orbital is used in resonance. 
1.5. 
(a) No by-products. C(1–3) and C(6–9) are the keys to numbering. 
(b) After numbering the major product, C6 and Br25 are left over, so make a bond between them and call it the 
by-product....
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Exam (elaborations) TEST BANK FOR The Art of Writing Reasonable Organic Reaction Mechanisms 3rd Edition By Robert B. Grossman (Solution Manual)-Converted
- Exam (elaborations) • 237 pages • 2021
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1.4. Furan has sp2 hybridization. One of the lone pairs is in a p orbital, and the other is in an sp2 orbital. Only 
the lone pair in the p orbital is used in resonance. 
1.5. 
(a) No by-products. C(1–3) and C(6–9) are the keys to numbering. 
(b) After numbering the major product, C6 and Br25 are left over, so make a bond between them and call it the 
by-product. 
1.6. (a) Make C4–O12, C6–C11, C9–O12. Break C4–C6, C9–C11, C11–O12. 
(b) Make C8–N10, C9–C13, C12–Br24. Break O...
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ACS Organic Chemistry Exam
- Exam (elaborations) • 8 pages • 2024
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What is the general formula for a carbohydrate? - Correct Answers: Cx(H2O)y 
 
How do you determine the number of stereoisomers for a given carbohydrate? - Correct Answers: 2^n where n= number of stereocenters 
 
Distinguish between the D and L designations for carbohydrates. - Correct Answers: In the L form the hydroxy group is on the bottom left closest to the CH2OH group in the frame of a Fischer projection 
In the D form the OH is on the bottom right 
 
What are anomers? - Correct Answe...
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Organic Chemistry 2: Summary of Aromatic Compounds
- Summary • 5 pages • 2022
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This document is a summary of the aromatic compounds chapter of the organic chemistry 2 course. It is digitally taken, handwritten notes. Notes in this chapter cover aromaticity, including Huckel’s number. 
It also includes a list of the most common aromatic compounds that must be memorized, naming di and tri substituted benzene derivatives. Lastly, it includes reactions on the side chain of a benzene ring, showing mechanisms as necessary as well as notes that further explain anything that ma...
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Diels-Alder Reaction
- Class notes • 3 pages • 2023
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5/4/2023 lecture notes, lecture 2 with Matt Bowman, Introductory Organic Chemistry I Spring Semester 2023
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