ORGANIC CHEMISTRY
5th Edition
ISBN: 9781259977596
Author: SMITH
Publisher: MCG
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Textbook Question
Chapter 1, Problem 1.19P
Using the principles of VSEPR theory, you can predict the geometry around any atom in any molecule, no matter how complex. Enanthotoxin is a poisonous compound isolated from a common variety of hemlock grown in England. Predict the geometry around the highlighted atoms in enanthotoxin.
Enanthotoxin
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Please answer part one and two, thank you!
Using the principles of VSEPR theory, you can predict the geometry or electron arrangement around any atom in any molecule, no matter how complex. Predict
the electron arrangement geometry around the indicated atoms in the structure shown.
a
H-C-0-H
Part 1 of 2
H
Part 2 of 2
b
H
Atom a: (Choose one)
linear
trigonal planar
tetrahedral
Atom b: (Choose one)
X
Which of the following explains the VSEPR geometry of an ammonia molecule?
It is trigonal pyramidal because there are four bonded pairs around nitrogen.
It is tetrahedral because there are four bonded pairs around nitrogen.
It is trigonal pyramidal because there are three bonded pairs and one lone pair around nitrogen.
It is tetrahedral because there are three bonded pairs and one lone pair around nitrogen.
Chapter 1 Solutions
ORGANIC CHEMISTRY
Ch. 1 - While the most common isotope of nitrogen has a...Ch. 1 - Label each bond in the following compounds as...Ch. 1 - How many covalent bonds are predicted for each...Ch. 1 - Draw a valid Lewis structure for each species. a....Ch. 1 - Draw an acceptable Lewis structure for each...Ch. 1 - Prob. 1.6PCh. 1 - Draw a Lewis structure for each ion. a. CH3Ob....Ch. 1 - Prob. 1.8PCh. 1 - Draw Lewis structures for each molecular formula....Ch. 1 - Classify each pair of compounds as isomers or...
Ch. 1 - Prob. 1.11PCh. 1 - Prob. 1.12PCh. 1 - Prob. 1.13PCh. 1 - Draw a second resonance structure for each species...Ch. 1 - Prob. 1.15PCh. 1 - Prob. 1.16PCh. 1 - Prob. 1.17PCh. 1 - Prob. 1.18PCh. 1 - Using the principles of VSEPR theory, you can...Ch. 1 - Convert each condensed formula to a Lewis...Ch. 1 - Prob. 1.21PCh. 1 - Prob. 1.22PCh. 1 - Convert each skeletal structure to a complete...Ch. 1 - What is the molecular formula of quinine, the...Ch. 1 - Draw in all hydrogens and lone pairs on the...Ch. 1 - Prob. 1.26PCh. 1 - What orbitals are used to form each of the CC, and...Ch. 1 - What orbitals are used to form each bond in the...Ch. 1 - Determine the hybridization around the highlighted...Ch. 1 - The unmistakable odor of a freshly cut cucumber is...Ch. 1 - Prob. 1.31PCh. 1 - Rank the following atoms in order of increasing...Ch. 1 - Prob. 1.33PCh. 1 - Prob. 1.34PCh. 1 - Provide the following information about...Ch. 1 - Use the ball-and-stick model to answer each...Ch. 1 - Citric acid is responsible for the tartness of...Ch. 1 - Zingerone gives ginger its pungent taste. a.What...Ch. 1 - Assign formal charges to each carbon atom in the...Ch. 1 - Assign formal charges to each and atom in the...Ch. 1 - Prob. 1.41PCh. 1 - Prob. 1.42PCh. 1 - Prob. 1.43PCh. 1 - Draw all possible isomers for each molecular...Ch. 1 - 1.45 Draw Lewis structures for the nine isomers...Ch. 1 - Prob. 1.46PCh. 1 - Prob. 1.47PCh. 1 - Prob. 1.48PCh. 1 - Prob. 1.49PCh. 1 - Prob. 1.50PCh. 1 - Prob. 1.51PCh. 1 - Prob. 1.52PCh. 1 - Consider compounds A-D, which contain both a...Ch. 1 - Prob. 1.54PCh. 1 - Prob. 1.55PCh. 1 - 1.56 Consider the compounds and ions with curved...Ch. 1 - 1.57 Predict all bond angles in each...Ch. 1 - 1.58 Predict the geometry around each highlighted...Ch. 1 - Prob. 1.59PCh. 1 - Draw in all the carbon and hydrogen atoms in each...Ch. 1 - 1.61 Convert each molecule into a skeletal...Ch. 1 - Prob. 1.62PCh. 1 - Prob. 1.63PCh. 1 - Predict the hybridization and geometry around each...Ch. 1 - Prob. 1.65PCh. 1 - Ketene, , is an unusual organic molecule that has...Ch. 1 - Rank the following bonds in order of increasing...Ch. 1 - Prob. 1.68PCh. 1 - Two useful organic compounds that contain Cl atoms...Ch. 1 - Use the symbols + and to indicate the polarity of...Ch. 1 - Prob. 1.71PCh. 1 - Anacin is an over-the-counter pain reliever that...Ch. 1 - Answer the following questions about acetonitrile...Ch. 1 - Prob. 1.74PCh. 1 - 1.75 The principles of this chapter can be...Ch. 1 -
a. What is the hybridization of each N atom in...Ch. 1 - 1.77 Stalevo is the trade name for a medication...Ch. 1 - 1.78 and are two highly reactive carbon...Ch. 1 - 1.79 The N atom in (acetamide) is hybridized,...Ch. 1 - Prob. 1.80PCh. 1 - Prob. 1.81PCh. 1 - Prob. 1.82PCh. 1 - Prob. 1.83PCh. 1 - Prob. 1.84PCh. 1 - Prob. 1.85P
Additional Science Textbook Solutions
Find more solutions based on key concepts
More than one choice may apply. Using the terms listed below, fill in the blank with the proper term. anterior ...
Essentials of Human Anatomy & Physiology (12th Edition)
What were the major microbiological interests of Martinus Beijerinck and Sergei Winogradsky? It can be said tha...
Brock Biology of Microorganisms (15th Edition)
2. Why is it that the range of resting blood pressures of humans is best represented by a bell-shaped curve co...
Human Biology: Concepts and Current Issues (8th Edition)
Give the IUPAC name for each compound.
Organic Chemistry
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- Methylcyanoacrylate is the active ingredient in super glues. Its Lewis structure is (a) Give values for the three bond angles indicated. (b) Indicate the most polar bond in the molecule. (c) Circle the shortest carbon-oxygen bond. (d) Circle the shortest carbon-carbon bond.arrow_forwardGroup X elements can conduct electricity and heat. As a chemistry student, Explain the characteristics of Group X elements. Explain the chemical properties of Group X elements . Discuss the trends of Group X elements when going down the group Using the knowledge of Lewis Diagram, show the formation of bond from any ONE of the element from Group X and any ONE non-metal element. State the electronic configuration of the cation and anion from the bond formed above. Draw the orbital diagram of the carbon and anion from thw bond formed above. Show the formation of positive ion and negative ion from the bond formed above and justify the differences in their number of electrons. Rubric: Part A; Choose your rubric based on the Bloom's. Part B; Assess originality.arrow_forwardPredict the ideal bond angles around each central atom in this molecule. PH oxygen: carbon: نیٹ H H H H O Oarrow_forward
- Predicting the arrangement of electron groups around the central atom of a molecule.arrow_forwardHow does adding an atom affect the position and angles of existing atoms or lone pairs? How does adding a lone pair affect the position and angles of existing atoms and lone pairs? Is the effect of adding bonded atoms and lone pairs to the central similar? Explain your answer. Describe what is meant by the "Steric #". Explain the difference between the terms "Electron Geometry" and "Molecule Geometry". How does changing a bond to a double or triple bond affect the shape of the molecules? List the molecules in Part III where the real bond angles differ from the theoretical model values. Why do you think the values differ?arrow_forwardDraw the 2D and the 3D Lewis structure for each molecule. You do not need to show resonance structures here. Determine the electron pair geometry (EPG), the molecular geometry (MG), the bond angle (BA) around the central atom, and the hybridization of the central or bold atom. Circle the formula of any polar molecule. For molecules with more than one central atom (e.g. CH3CH20H) give the structure around the bold atom. Molecule ЕPG Hyb (circle if 2D Lewis Structure 3D Lewis Structure MG polar) ВА CH2S GeO2 CF4arrow_forward
- Please answer the following questions about the below molecule: This molecule has ___ sigma bonds. This molecule has ___ pi bonds. This molecule has ___ hydrogen atoms. This molecule has ___ carbon atoms. This molecule has ___ lone pairs The nitrogen atom is ___ hybridized. The ___ orbital is involved in all hydrogen sigma bonding. The bond angle of C-N-O is ___ °.arrow_forwardDepending on the protein under study, the bond angle of a drug molecule can become critical to successfully deactivating a viral protein. For this reason, chemists are frequently concerned with the 3D shape of their molecules and their bond angles. The oxygen atom shown in the structure has a tetrahedral electronic geometry, meaning we would predict that it would have 109.5° bond angles. However, the actual structure, the bond angles are smaller than 109.5°. Explain why this compression occurs. Make sure to discuss what’s happening around/what groups are present around the oxygen atom.arrow_forwardMark the correct statements related to the bonding, shape and polarity of molecules. A - Only valence electrons are used when Lewis structures are drawn. B - Valence electrons occupying pi bonding orbitals are not considered when determining the molecular shape with the VSEPR theory C- The lone pairs on the central atom does not influence the molecular shape of a molecule. D- Molecules with polar bonds are polar. E - Molecules with a tetrahedral electron pair geometry are non-polar.arrow_forward
- In addition to the items required for part A, divide the naming of the geometry into a name for the arrangement about each atom that can be considered central to two or more it is bound to. Make only one overall ball-and-stick sketch and judge overall polarity. Fill in the blanks here!arrow_forwardName Section Table 1: Complete this table with your partner. You may ask the instructor to check your work. Formula Lewis structure Molecular geometry and bond angle(s) around central atoms(s) Polar or nonpolar, draw dipole arrow Hybridization of each atom Orbitals involved in each bond CO2 2 x C=O: sp- sp o o=c=o° C: sp O: sp Linear, 180° Non-polar 2 x C=O: p-p TC COF2 CH2CH2 SCI2 SF4 atoms. atomarrow_forwardPlease envision this table like it was one long table. (I had to make it two because it hung out of the quiz boundaries and was inaccessible.) It is recommended that you draw the Lewis Structure of the molecules and then complete this table. electronic Molecular Molecule Geometry Geometry CH3F tetrahedral tetrahedral NH3 tetrahedral trigonal pyramidal C2F4 trigonal planar trigonal planar CO2 linear linear main dipole Molecule intermolecular moment force CH3F [ Select ] yes NH3 hydrogen bonding yes C2F4 [ Select ) no CO2 ( Select | no > >arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
Chemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
Chemistry: Matter and Change
Chemistry
ISBN:9780078746376
Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom
Publisher:Glencoe/McGraw-Hill School Pub Co
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Stoichiometry - Chemistry for Massive Creatures: Crash Course Chemistry #6; Author: Crash Course;https://www.youtube.com/watch?v=UL1jmJaUkaQ;License: Standard YouTube License, CC-BY
Bonding (Ionic, Covalent & Metallic) - GCSE Chemistry; Author: Science Shorts;https://www.youtube.com/watch?v=p9MA6Od-zBA;License: Standard YouTube License, CC-BY
General Chemistry 1A. Lecture 12. Two Theories of Bonding.; Author: UCI Open;https://www.youtube.com/watch?v=dLTlL9Z1bh0;License: CC-BY