Part III. Clearly place a box around the most positively charged sp³ hybridized carbon in THC. hybridized atoms in THC. [Concept: hybridization). [Concepts: hybridization, bonding). Part IV. In the space below, draw all the resonance structures of THC. CH, SOH H HC H₂C H HC-то H3C Н H=C HIC ICti> 04 Loo Kui It : alt : OH (H₂ CH3 сн Н H=C H H нх СН3 H H₂c ar HE TO H3C 1 CH3 st H in H H PH | CH₂ OH : Ol
Electronic Effects
The effect of electrons that are located in the chemical bonds within the atoms of the molecule is termed an electronic effect. The electronic effect is also explained as the effect through which the reactivity of the compound in one portion is controlled by the electron repulsion or attraction producing in another portion of the molecule.
Drawing Resonance Forms
In organic chemistry, resonance may be a mental exercise that illustrates the delocalization of electrons inside molecules within the valence bond theory of octet bonding. It entails creating several Lewis structures that, when combined, reflect the molecule's entire electronic structure. One Lewis diagram cannot explain the bonding (lone pair, double bond, octet) elaborately. A hybrid describes a combination of possible resonance structures that represents the entire delocalization of electrons within the molecule.
Using Molecular Structure To Predict Equilibrium
Equilibrium does not always imply an equal presence of reactants and products. This signifies that the reaction reaches a point when reactant and product quantities remain constant as the rate of forward and backward reaction is the same. Molecular structures of various compounds can help in predicting equilibrium.
What are all nine resonance structures for tetrahydrocannabinol (thc) ?
![ОТСОН
2022
rt 1. Write out the complete molecular formula of THC and CBD. Are these molecules constitutional
omers? [Concept: Lewis Structure]
THC = (C, H)3 Ог
CBD =
н
(ст Нодь Ог
Part II. Clearly circle all of the sp² hybridized atoms in THC. [Concept: hybridization).
[Concepts: hybridization, bonding].
Part III. Clearly place a box around the most positively charged sp³ hybridized carbon in THC.
Part IV. In the space below, draw all the resonance structures of THC.
C₁H₂
애
H=C
H
HC-
H
H3C
H3C
Н
HC Hхс
CH₂
H3C
СН3
H₂C
(CH,
НЗС НЗС
Снз
оч
: alt
он
이
L
-
CH3
Е
и сн
-
CH3
- сн
isomers ? (circle one answer)
YES
- (H3
Н
Н
H=C
Н
H3C
H
H₂C
СН3
H3c
HS →
NO
H3C
H
H3C
(H 3
СН3
унто н
H₂(
рон
CH3 :olf
H=C
H
82
(H3
H₂C
애
14
애
olf
2)
CH₂
<
- сно
-)
(Hs
2
- сн
(H)](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F927ccd5f-a2a8-46df-9933-bf1a0a6d56eb%2Fa7930500-56ee-4aee-a86e-45ed65ea9fa3%2Ffkzn5ap_processed.jpeg&w=3840&q=75)
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