What is Resonance Theory? Sate five conclusions that can be drawn from the theory. 2.State the two main experiments that were used to establish the extra stability of the benzene molecule. 3.What are the factors that confer Aromaticity to an organic molecule? 4.i. State the effects of substituents on a benzene derivative towards further aromatic substitution. ii.Based on the above suggest the various types of substituents that can be attached to Benzene.

What is Resonance Theory? Sate five conclusions that can be drawn from the theory. 2.State the two main experiments that were used to establish the extra stability of the benzene molecule. 3.What are the factors that confer Aromaticity to an organic molecule? 4.i. State the effects of substituents on a benzene derivative towards further aromatic substitution. ii.Based on the above suggest the various types of substituents that can be attached to Benzene.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter18: Aromaticity

Section: Chapter Questions

Problem 7CTQ

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1 i. What is Resonance Theory? Sate five conclusions that can be drawn from the theory. ii. State the two main experiments that were used to establish the extra stability of the benzene molecule. iii. What are the factors that confer Aromaticity to an organic molecule? iv. State the effects of substituents on a benzene derivative towards further aromatic substitution. V. Based on the above suggest the various types of substituents that can be attached to Benzene.
What is Resonance Theory? Sate five conclusions that can be drawn from the theory. State the two main experiments that were used to establish the extra stability of the benzene molecule. What are the factors that confer Aromaticity to an organic molecule? i. State the effects of substituents on a benzene derivative towards further aromatic substitution. Based on the above suggest the various types of substituents that can be attached to Benzene. What are the various ways by which alkenes may be synthesized? i. Give two examples each of Unsymmetrical alkenes and reagents. Give two examples of reactions of alkenes that result in Anti-Markonikov’s addition products
Why was the formal charge of (+) placed on this carbon? I understand everything else about the question but can someone help me with explaining this. Thanks!
1. What is resonance theory? State five conclusionstgan can be drawn from the theory. 2.What factors confer aromaticity to an organic molecule. 3. What are the various ways by which alkenes can be synthesized. 4. State the two main experiment that were used to establish the extra stability of the benzene molecule.
View the first compound name provided in Table 6. Follow the steps below and draw each part of the structure on a piece of paper. Determine the number of carbons present in the compound based on the base name. Draw the carbon chain and include any double or triple bonds if indicated in the suffix of the base name. Number each carbon. The carbons can be numbered from left to right or right to left. Draw any substituents on the corresponding carbon atom for which is indicated in the name. Refer to Figures 3 and 4 in the background for a visual representation of numbered carbons with corresponding substituents. Check that each carbon atom has a total of 4 bonds.
Answer the following true or false questions about the molecule acrylaldehyde, its resonance structures, and resonance hybrid. In fairness, many of these statements are false and represent common misconceptions about resonance. If a statement is false as written, change the underlined fragment of the statement to make it true 4) The pair of electrons labeled “A” (at the end of the arrow) are localized 5) The pair of electrons labeled “B” (at the end of the arrow) are delocalized 6) The pair of electrons labeled “C” (at the end of the arrow) are localized
Give a clear handwritten answer with more explanation about given molecules..?
Question (Organic Chemistry) Consider molecules A–B. Does the arrow pushing in each structure leadto an acceptable resonance form? If so, explain why it is acceptable or unacceptable? What are the rules and logic? If so, draw it and carefully explain your answer and provide explanations for why each structure leds to an acceptable or unacceptable resonance form. Why is the arrow pushing acceptable or unacceptable in each individual case? Explain you answer with many details, logic, and in a step-by-step fashion. Please explain your rationale or logic. The answers provided on Bartleby lack a clear rationale and explanation of why the octet rule matters or why electron rich and electron deficient sites are important to this drawings.
for part b）why do we write AlCl3 at top of the arrow and AlCl4 at the bottom of arrow？？is it any connection between the two？does it means that AlCl 4 need to be present in order to make AlCl3 reacts to the molecule and make the reaction to process？？ 2. why when AlCl3 added，Cl was removed from the ring？what princeiple theory is that ？ 2. when SO3 is added ，SO3 attached to the ring，why ？what principle is behind this phenamonane 3.Just confused about why AlCl3 removes Cl from the ring，while HSO3 donate SO3 to the ring. Is it Something about nucleohilic or eletrciohillic？
Question (Organic Chemistry) Consider molecules A–B. Does the arrow pushing in each structure leadto an acceptable resonance form? If so, explain why it is acceptable or unacceptable? What are the rules and logic? If so, draw it and carefully explain your answer and provide explanations for why each structure leds to an acceptable or unacceptable resonance form. Why is the arrow pushing acceptable or unacceptable in each individual case? Explain you answer with many details, logic, and in a step-by-step fashion.
help fill out this sheet based on structure
I am confused as to how to do this problem. Does the double bond change anything?