Answered: cation Draw a resonance structure of…

cation Draw a resonance structure of this subsituted cycloheptatrienyl that has the same number of pi bonds as the original structure. Include all lone pairs in your structure.

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...

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Concept explainers

Alkynes

Alkynes are organic compounds that contain at least one triple bond between carbon-carbon atoms. They are a series of unsaturated compounds with a general molecular formula, CnH2n-2.

Question

cation
Draw a resonance structure of this
subsituted cycloheptatrienyl
that has the same number of pi
bonds as the original structure.
Include all lone pairs in your
structure.
HCO
Drawing
I
1

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The bond dissociation energy of one of the C–H bonds is considerablyless than the bond dissociation energy of the other. Which C–H bondis weaker? Offer an explanation.
8. Using Zaitsev's rule, choose the most stable alkene among the following. Draw out the structures of each of the options then select the correct answer. Recall that Zaitsev's Rule is about alkene stability. The trend for this is similar to the trend for carbocation stability. Either more or fewer groups on the alkene (and the carbocation) make it more stable. This question is wanting you to remember if more or fewer. it's A) 1,2-dimethylcyclohexene B) 1,6-dimethylcyclohexene C) cis-3,4-dimethylcyclohexene D) They are all of equal stability according to Zaitsev's rule. hat
2. Draw the 1,2-addition and the 1,4-addition products for each of the following reactions. Label the major and minor product for each reaction. Reagents/Conditions 1,3-butadiene 1,3-butadiene 2,4-hexadiene 1,3-hexadiene 1,3-pentadiene 1,3-cyclopentadiene 1,3-cyclohexadiene REACTIONS OF DIENES 2,4-octadiene HBr -80 °C HBr 40 °C HI -80° C HI 40 °C Br₂ 40 °C Br2/H₂O 60 °C Br₂ -20° C Br2/H₂O 60 °C 1,2-addition (kinetic) 1,4-addition (thermodynamic)
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Provide structural(constitutional) isomers and resonance structures. Also, provide chemical formula and electron movement of resonance structures.
2
Don't use hand raiting please
Please answer d and e.
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.
None
2. Why do 1-methylcyclohexene and 3-methylcyclohexene have a lower boiling point than 2-methylcyclohexanol?