For a compound to be aromatic a molecule should follow hund rule
1 -conjugation in a molecule must be present
2 should be planar
3-(4n+2) pi electrons must be present
So in question 2 a molecule follow all three rulesso option d is correct
Q-3 option a is correct ....in this molecule hunds rule is not followed
Question 2 (1 point) Select all TRUE statements about the molecule below: A) This molecule obeys...
Which of the following statements is not true for a compound to be considered aromatic? Select one: O a. the compound must be monocyclic b. the compound must have 4n + 2 pi-electrons delocalized over the ring system O c. the compound must have conjugated p-orbitals at ever atom of the ring o d. the compound must be planar
Use the following list of compounds to answer the following questions Select the compound that is best described as: (a) A neutral system, 4x electrons, anti-aromatic (b) A 6 electron aromatic system. (C) An aromatic system because n = 2 in Huckel's rule 4n+2 (d) A 6 electron conjugate non-aromatic system (e) An unconjugated hydrocarbon. (1) Not aromatic as it is drawn, but if removed, it would aromatic cation (6) Not aromatic as it is drawn, but it has a...
Which of the following statements correctly applies Hückel's rule to the molecules shown below? Molecule 4 is weakly basic, therefore it cannot be aromatic. Molecule 5 has 8 electrons Otherefore it cannot be aromatic Molecule 2 is not a hydrocarbon; therefore it cannot be aromatic. Molecule 3 is not completely conjugated; therefore it cannot be aromatic Molecule 1 is not monocyclic; therefore it cannot be aromatic
Which of the following statements correctly applies Hückel's rule to the molecules shown below? -CH=CH2 H 2 3 5 O Molecule 2 is not a hydrocarbon; therefore it cannot be aromatic. O Molecule 1 is not monocyclic; therefore it cannot be aromatic. O Molecule 4 is weakly basic; therefore it cannot be aromatic. Molecule 3 is not completely O conjugated; therefore it cannot be aromatic. Molecule 5 has 8 electrons; therefore it cannot be aromatic.
2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect this molecule to be aromatic, antiaromatic or non aromatic? Explain. (3pts) 16 Te 1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sn2 hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts)
Which statements about IS3+ ion is NOT true. A. The molecule has non-polar bonds and is a non-polar molecule. B. The molecule has trigonal planar geometry. C. The central atom does form double or triple bonds. D. There are two ore more resonance structures for the molecule E. The central atoms Violates the octet rule by accepting more than an octet of electrons.
sify each of the statements about the octet rule as true or false. True False Answer Bank Atems with eight valence electrons follow the octetrue. Hemen in group 1 A (I) of the periodic table will gain one electron to form an excel Nl of the elements in group A (1) of the periodic table obey the ostet rule. Only woms with eactly eight electrons follow the octer rule. c about o ntact us hele 80 H C 5 of...
For each of the species below, identify any cyclic conjugated system, then: 1. Determine the number of electrons in a system of cyclic conjugation (zero if no cyclic conjugation). 2. Specify whether the species is "a"-aromatic, "aa"-anti-aromatic, or "na"-non-aromatic (neither aromatic nor anti-aromatic). (Presume rings to be planar unless structure obviously prevents planarity. If there is more than one conjugated ring, count electrons in the largest.) please help with these study guide questions; I always thumbs up, thank you for...
please answer the question above 1. Identify any true statements about the following molecule. ÇO2H H- OH HOH COZH Select all that are True. The molecule is a meso compound The molecule is achiral The molecule is optically inactive The molecule has an enantiomer The molecule is chiral The molecule has at least one diastereomer Submit Answer Tries 0/1
Question 2 1 pts Determine if each of the following statements is True or False about sigma (o) bonds and pi (Tt) bonds. 1) A single bond could be either a sigma (a) bond or a pi (rt) bond. (Select] 2) A sigma (o) bond could be formed when an sorbtial and a porbital overlap end-to-end. [Select) 3) Sigma (o) bonds can be formed by the overlap of an orbital and a hybrid orbital. [Select] 4) The picture below represents...