Can someone explain how to get the following: h(1)-0(2)-c(3) bond angle? also, determine the hybridization of O(7), H(11), C(10) & C(5) The image shows the molecular structure of aspirin with atoms numbered for reference. Here is a detailed explanation of the structure:- The structure is based on a benzene ring, shown as a six-membered carbon (C) ring with alternating single and double bonds.- Each carbon atom in the benzene ring is bonded to a hydrogen (H) atom. The hydrogens are not numbered in this depiction.- The functional groups are as follows:1. A carboxyl group (COOH) is attached to one carbon of the benzene ring: - Atom 1 is a hydrogen (H). - Atom 2 is an oxygen (O) with a double bond to the central carbon (atom 3). - Atom 3 is the carbon (C) bonded to the benzene ring. - Atom 4 is an oxygen (O) with a single bond to the central carbon (atom 3) and carries a lone pair of electrons.2. An ester group (COO) is attached to the benzene ring: - Atom 5 is part of the benzene ring and has branching atoms. - Atom 6 is a carbon (C) that connects to atom 7. - Atom 7 is an oxygen (O) double-bonded to atom 6. - Atom 8 is another oxygen (O) connected to the benzene ring. - Atom 9 is a carbon (C) bonded to atom 8 and part of the methyl group. - Atom 10 is an oxygen (O) with a lone pair of electrons, connected to atom 9. - Atom 11 is a hydrogen (H) bonded to the methyl group.- Lone pairs of electrons are depicted as dots around the oxygen atoms at positions 4, 7, and 10. This molecular configuration illustrates the basic functional components of aspirin, which is an acetylated form of salicylic acid, imparting it with its anti-inflammatory properties.

Answered: Can someone explain how to get the…

Can someone explain how to get the following: h(1)-0(2)-c(3) bond angle? also, determine the hybridization of O(7), H(11), C(10) & C(5)

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...

See similar textbooks

Similar questions

2) Considered the following molecules: Draw the valence electron configuration of each atom (including their spin direction) and circle each pair of electrons that make a bond within the molecule. Determine the hybridization state for each carbon atom. Then draw the Lewis Structure and count how many bonds are sigma or pi bonds a) H₂CO b) C2F2
Please confirm if my answer is correct or not. Due to the need for this to be correct I would like you to provide me with a confidence score in you answer on a scale from 1 to 10 how confident are you in your answer. Please be sure to double check your answer
For the molecule shown below, identify the hybridization on the C atom with the double bonded oxygen and the approximate bond angle labeled beta: Group of answer choices hybridization: sp2 bond angle: 120° hybridization: sp3 bond angle: 109.5° hybridization: sp3d bond angle: 90° hybridization: sp3 bond angle: 120°
2) Which of the following arrangements of p atomic orbitals gives the lowest energy л- antibonding molecular orbital of 1,3-butadiene? 8888 8888 2 3
Draw a 3D representation of the molecule penta-1,2,3,4-tetraene using the following EXPLICIT instructions: sigma bonds in the plane of the paper are normal lines, sigma bonds or orbitals projecting in front of the page are heavy lines, sigma bonds or orbitals projecting behind the page are dashed lines, and pi bonds are shown by drawing the lobes of the p-orbitals and indicating the overlaps. What is the hybridization of each atom (except H) in this molecule?
10. Which of the following DOES NOT represent the appropriate hybridization state of the carbon atoms in the structures shown below? A) B) C) D) CH₂OH ; H- H sp³ hybridized C FN-H ; CHFBrI ; sp² hybridized H-CEN ; sp hybridized sp 4 hybridized
20. Which of the following statements about hybridization is FALSE? A) The ideal angle between sp³-hybridized orbitals is 109.5º. A 3s orbital is spherical with no nodes. B D) E) Carbon is not the only atom that undergoes hybridization. Mixing three atomic orbitals always results in the formation of three orbitals. In carbon, electrons in an sp²-hybridized orbital are higher in ener an sp-hybridized orbital. 21. Which of the following statements about Aspartame (sh НО. NH₂ re 6 n-bonds. 2-hybridized c bonds O
The sp3 hybridization is associated with which of the following molecular geometries? Select the correct answer below: octahedral tetrahedral linear trigonal planar
9. (a) hexamethyltungsten, [W(CH3)]. Assume perfect Dan symmetry and include the correct orbital overlap. (b) geometry? Draw the full molecular orbital diagram for the trigonal prismatic, Why is there an overall net gain in energy compared to the octahedral CH3 CH3 CH3 CH3
2) a) Consider the following molecule . Given what you have learned about hybridization theory, draw an image or images explaining the bonding situation in this molecule. I want you to draw out all of the orbitals, hybrid orbitals and how they overlap to form the bonds in the molecule. Indicate the % s or p character in the given atomic and hybrid orbitals. Which C-C bond or bonds are the longest? In a paragraph or so explain the image or images you just drew. b) Lastly, consider the molecule below. Indicate the Molecular formula, the molar mass, label the hybridization of each atom except for hydrogen, indicate any chiral centers with a *, which bond or bonds are the shortest, identify by name of each functional group with an arrow pointing to the group.