7. Draw curved arrows indicating the movements of electrons between the following pair ofresonance structures. Name the pattern of resonance shown. What is the hybridization of thecarbon atoms?8. Draw the remaining three resonance structures for the molecule in problem 7 above.9. There are several possible forms of a trisubstituted cyclohexane with the formula C10H200. Ihave drawn four of them. From these, which one do you think is most commonly naturallyoccurring, and why? Which is least commonly occurring and why?HOHO"HOHO

Since you have posted unrelated multiple questions, hence answering only first 2 related ones.

7. Draw curved arrows indicating the movements of electrons between the following pair of resonance structures. Name the pattern of resonance shown. What is the hybridization of the carbon atoms? 8. Draw the remaining three resonance structures for the molecule in problem 7 above.

7. Draw curved arrows indicating the movements of electrons between the following pair of resonance structures. Name the pattern of resonance shown. What is the hybridization of the carbon atoms? 8. Draw the remaining three resonance structures for the molecule in problem 7 above.

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...

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Table 2 Duplicate this table, scan, and upload as an attachment. Molecular Polar Draw Lewis Structure Hybridization of Formula Center Atom Y/N? N3 co,? BFA CH,CH, (2 carbon centers) CHCH (2 carbon centers)
5. Follow the curve arrows in the image below and draw the correct second resonan structure.
O REPRESENTATIONS OF ORGANIC MOLECULES Understanding how to make sp hybrid orbitals Examine the picture in the box below. Select the atomic orbitals in the table below that would blend together to produce the set of hybrid orbitals pictured in the box. If at least one orbital is missing to make the pictured hybrid set, select "missing atomic orbitals". p missing atomic orbitals 3/5 X
Allenes are molecules that have multiple double bonds in a row. Below are the condensed structure and a figure showing valence-bond theory for the orbital overlap in the simplest allene. H,C=c=CH, 1. Using the condensed structure, indicate the hybridization for each carbon. 2. Using the condensed structure, indicate the molecular geometry for each carbon. 3. How many o bonds are there in this allene? 4. How many n bonds are there in this allene? 5. Draw a 3-D structure for this allene.
1. For each molecule and ion below, indicate the total number of valence electrons. Based on that number of electrons, draw a valid Lewis structure.2. Use VSEPR theory to determine the electron arrangement and the geometry of the molecule around the central atom(s). A table of geometries is attached.3. Build the molecule using the molecular models provided in the lab. Sketch your model well enough to show the geometry. Include bond angles.4. Using your understanding of electronegativity and its trends in the Periodic Table, determine if polar bonds exist in the molecule.5. Using bond polarity and molecular shape, determine if the molecule has an overall dipole. If all the bonds are nonpolar, the molecule is nonpolar. If polar bonds are present, then consider the shape to determine if the molecule has an overall dipole.
What is the number of sp hybridized carbon atoms on the given structure? Just type the number. For example, 1 H2C ECH H3C
1. Tamiflu is a prescription medication used to treat the flu. What is the hybridization state, molecular geometry and approximate bond angle at the indicated carbon, oxygen, and nitrogen atoms? III NH₂ II 2. Identify the orbitals that are overlapping to form each of the bonds indicated by the arrows below.
3) Isodihydrohistrionicotoxin, shown below, is a toxin found in the skins of poison dart frogs from South and Central America. The picture is an example of a strawberry poison dart frog. On the structure below, please identify the hybridization of the atoms that are circled. Write the hybridization of the circled atoms in the boxes provided. OH HN The dot represents a carbon
CHOOSE THE CORRECT NUMBER CORRESPONDING TO THE RIGHT ANSWER PLEASE Formed when the electron being shared come only from one of the elements. coordinate covalent bond pure covalent bond polar covalent bond non-polar covalent bond The hybrid orbital which has one fourth s character and three fourths p character. sp sp2 sp2 special sp3 The number of sigma bonds in sp2 hybridized carbon. 1 2 3 4 Hybridization of oxygen in furan. sp sp2 sp2 special sp3 The number of sigma bonds in an sp2 hybridized oxygen. 1 2 3 4 He believed that matter is continuous and can be divided into smaller particles John Dalton Aristotle Democritus Leucippus Which of the following factors does not affect bond energy? bond polarity orbital hybridization formal charge loss of overlap Calculate the formal charge of sulfur in sulfuric acid 0 -2 2 6 Bond angle between two sp3 hybridized orbitals. 60 degrees 5 degrees 120 degrees 180 degrees Pi bonds can be formed by the overlapping of the…
4 of 4 7. Circle each of the molecule(s) below that have a a bond made from the overlap between an sp-hybridized orbital and an sp²-hybridized orbital. 8. Levomenol is a naturally occurring molecule with a sweet aroma that is used in many fragrances; it also has antimicrobial and anti-inflammatory properties. Identify the number of hybridized atoms in each category (sp, sp², sp³), o bonds, bonds, lone pairs, and implied hydrogen atoms. H OH Levomenol 9. Answer the questions below about the following molecules. A CI HO sp sp² sp³ B In which molecule would you expect the C-Cl bond to be stronger? In which molecule would you expect the C-Cl bond to be shorter? What is the geometry of the C atom in the C-Cl of molecule A? What is the geometry of the C atom in the C-Cl of molecule B? T lp H 10. The following molecule is bombykol (a naturally occurring pheromone formed in silk worms), assign a geometry and bond angle to each non-hydrogen atom.
a) Draw the Lewis structure for CH,F2. lit. b) What is the shape or geometry at the center atom? c) What is the bond angle at the center atom? Enter a plain number, but include the "<" sign in front if needed. d) What is the hybridization at the center atom? Enter without superscripts. For instance, if it were sp', you would type "sp3". e) Is the molecule polar or nonpolar overallI? Type "polar" or "nonpolar".
Write 1)compound name 2)number of bonding electron pairs(bp)/number of lone electron pairs(lp) 3)electron dot(Lewis) structure 4)molecular geometry/electron dot geometry 5)dipole moment(yes or no) 6)central atom hybridization/ bond angle(s)