Caffeine is an aromatic compound.Using resonance structures, showhow the sixmember ring can bedrawn in its "benzoid" form. Indicatethe hybridization of each nitrogenatom and specify the hybridization ofthe orbital occupied by each of thelone pairs.Write all possiblereasonable resonance structures forthe following compounds. Labelthe major and minor contributors toeach resonance hybrid.N: Z—N:

Step 1: Step 2:In the six-sided ring, all the nitrogen atoms are sp² hybridized.The lone pairs of…

Answered: Caffeine is an aromatic compound. Using…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter3: Electron Orbitals

Section: Chapter Questions

Problem 8E

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Answer it please;
what is the reasonance structure of this?
Lewis structures of mescaline, a hallucinogenic compound in peyote cactus, and dopamine, a neurotransmitter in the mammalian brain, appear below. Suggest a reason for mescaline’s ability to disrupt nerve impulses.
Draw an orbital picture of thiazole. Assume that both the nitrogen and sulfur atoms are sp2-hybridized, and show the orbitals that the lone pairs occupy.
(b) (ii) types of bonds between carbon and nitrogen a character in character (iii) type of orbital that contains the lone electron pair on nitrogen ++* H H- (1) hybridization of C and N C [References]
Exhibit 1-3 Determine the hybridization for the indicated atoms in each structure below. A B. :0: || CH;—CH,—C-0H Refer to Exhibit 1-3. The hybridization of this oxygen atom (B) is
3) How many electrons are delocalized in how many p-orbitals? Draw the most and second most stable resonance structures of the following compound. Order the structures by increasing stability. What is the partial charge distribution in the resonance hybrid?
The calicene molecule has a different dipolar moment of 0 and also thedipole points to the larger ring. Draw a structure resonance where you can see that distribution of loads and using the concept of aromaticity and resonance structures, explain why the moment dipolarit's different from zero
Give correct detailed Solution with explanation needed..don't give Handwritten answer
(a) Identify which atomic orbitals are used to construct the specified o bonds: Bond a is: b Bond a is: OH bond b is: Identify which orbital is used to construct the л-bond at the marked atom. (b) Identify which atomic orbitals are used to construct the specified & bonds: a and bond c is: OH bond b is: and bond c is: Identify which orbital is used to construct the л-bond at the marked atom.
H genistein HO, H H : ОН HO, H (a) Is the hybridization of each C in the right-most ring the same? Explain. (b) Is the hybridization of the O atoms in/on the center ring the same as that of the O atoms in the OH groups? Explain. (c) How many carbon-oxygen o-bonds are there in genistein? How many carbon-oxygen n-bonds? (d) Do all the lone pairs on the oxygens occupy the same type of hybrid orbital? Explain by labeling the hybridization of each oxygen atom in genistein.

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