There are four aromatic compounds present.
They are options 1,2,4, and 5.
option 1 has 5 double bonds = 10 pi electrons ( 4*2 + 2 = 10 so it obeys 4n+2 rule)
option 2 has 2 double bonds and in O there are two lone pair of electrons among two lone one pair involves delocalization pi electrons hence total 6 electrons in cyclic delocalization ( 4*1 +2 = 6)
option 4 has 2 pi bond ( 4 pi electron ) and one lone pair electron on carbon with negative charge so total 6 electron
option 5 has 7 double bond = 14 electron ( 4*3 +2 = 14)
According to the general definition of aromaticity and the Hackle's 4n + pi rule, predict the...
Aromaticity Worksheet CHEM 2410 Fall 2019 Determine if the following compounds are aromatic, anti-aromatic or non-aromatic. Give reasons for your answer. ***Assume all the cyclic compounds are planar (flat) for these problems. Summary Notes: Aromatic - 4n+2 pi electrons, complete cyclic conjugated pi system and planar (flat) Anti-aromatic - 4n pi electrons, ccyclic conjugated pi system and planar(flat) Non-aromatic - breaks any of the above rules (all other compounds) Sp3 hybridized heteroatoms (O, S, N) are involved in the pi...
Aromaticity Worksheet CHEM 2410 Fall 2019 Determine if the following compounds are aromatic, anti-aromatic or non-aromatic. Give reasons for your answer. ***Assume all the cyclic compounds are planar (flat) for these problems. Summary Notes: Aromatic - 4n+2 pi electrons, complete cyclic conjugated pi system and planar (flat) Anti-aromatic - 4n pi electrons, cyclic conjugated pi system and planar(flat) Non-aromatic-breaks any of the above rules (all other compounds) Sp3 hybridized heteroatoms (O, S, N) are involved in the pi system Sp2...
2. Which of the following pi electrons in a cyclic compound meet the criteria of Hückel's rule? a. 4N b. 6N C. 4N42 d. 6N+2 3. From the following compounds having 10 pi electrons that meet Huckel's rule, circle on the aromatic ring. ??
e 2. One of the criteria for aromaticity is that That is, you can draw resonance structures the following aromatic compounds draw ALL resonance structures to su completely conjugated around the ring. The fi aromaticity is that the pi clectrons in a flatring are completely conjugac mance structures that delocalize pi clectrons completely around the ring conjugated around the ring. The first example has been completed as a reieck sonance structures to show how pi electrons are 1 . 1...
1. (a) (10 points) Give the number of pi electrons and determine whether each of the following compounds is aromatic, anti-aromatic, or non aromatic. compound number of x electrons aromaticity cyclohexatrienyl dianion
2. Increasing the aromaticity of by fusing more benzene rings together forms a special class of compounds that are called Polycyclic Aromatic Hydrocarbons (PAHs). Primary sources of these compounds are from burning coal, gasoline, wood and trash. These compounds are very persistent organic pollutants and are carcinogenic. We will predict their UV-Vis properties using the Particle-in-a-2- D box model. For the following two aromatic compounds, calculate the wavelength corresponding to the lowest energy wavelength. Should it be a colored compound?...
3. Predict if the following compounds are aromatic, antiaromatic, or nonaromatic by using Hückel's Rule. (9 points) NH O tto stavio 0
2) Use your knowledge of resonance, aromaticity, and general stability trends to analyze the following reaction provide your reasoning why that reaction is fast or slow (1 point) Reasoning: Ho NaNH2 HH Chemistry of Aromatic Com slow pka = 36 HH NaNH2 fast pka = 16
Which of the following structures qualify as being aromatic, according to Huckel's rule? Note: If one or more structures are incorrectly placed, a single red X will appear on the top left. Which of the following structures qualify as being aromatic, according to Huckel's rule? Note: If one or more structures are incorrectly placed, a single red X will appear on the top left. Not Aromatic Aromatic 2K