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.

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.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Which structure is aromatic and has six electrons In the conjugated system? Click on a letter A through D to answer. H A. C. D. В.
p
A benzene ring alters the reactivity of a neighboring group in the so-called “benzylic” position, similarly to how a double bond alters the reactivity of groups in the “allylic” position. Benzylic cations, anions, and radicals are all more stable than simple alkyl intermediates. a) Use resonance structures to show the delocalization of the positive charge, negative charge, and unpaired electron of the benzyl cation, anion, and radical.
2. Draw the structures for the following molecules given their IUPAC names. a.) 3-chloro-2-methylpropanoic acid b.) 3-chloro-1,1-cyclopentanedicarboxylic acid c.) 3,3-dimethylheptanoic acid d.) Cesium 3,3,-dimethylheptanoate
Explain the role strain plays on stability and reactivity of a cyclic alkane such as cyclopropane.
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 4 and 5 in the background for a visual representation of numbered carbons with corresponding substituents. Check that each carbon atom has a total of 4 bonds.
What is the IUPAC name of the following compound? F. а. 1-ethyl-3-fluoro-2,5-dimethylcyclohexane O b. 2-ethyl-6-fluoro-1,4-dimethylcyclohexane c. 3-ethyl-5-fluoro-1,4-dimethylcyclohexane O d. 3-ethyl-1-fluoro-2,5-dimethylcyclohexane Jump to... nework
Industiral Chemistry Both Tetraethyl lead and methyl-t-butyl ether have been removed from or in the process of being removed from the gasoline additive industry. Explain why each of these compounds were used so highly, and why each is considered dangerous.