Introduction to General, Organic and Biochemistry
11th Edition
ISBN: 9781285869759
Author: Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Textbook Question
Chapter 10, Problem 10.42P
Silicon is immediately below carbon in Group 4A of the Periodic Table. Predict the C—Si—C bond angles in tetramethylsilane, (CH3)4Si.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Compare the polarity of the C-Cl bond in (CH3)3C-Cl with the polarity of the Si-Cl bond in (CH3)3Si-Cl.
Structural Isomers: Alkanes
One of the reasons for the complexity of carbon compounds is that it can bond (catenate) with itself. Oils are mostly made up of hydrocarbons, for 'saturated' compounds, these obey the formula CnH2n+2. The empirical formula (unlike benzene) will vary with n. Now we have established C is tetrahedral, how many structural (skeletal) isomers can we find for n=6, hexane C6H14 ?
1) Sketch all the isomers. What procedure did you use to make sure you didn’t miss any ? Do you think you could you do this now for heptane C7H16 ?! (Hint: 9 different ‘skeletal’ topologies)
Note the number of possible isomers increases in highly exponential way. C10 – 75 isomers C15 – 4,347 isomers C20 - 366,319 isomers !!
Note:-
• Do not provide handwritten solution. Maintain accuracy and quality in your answer. Take care of plagiarism.
• Answer completely.
• You will get up vote for sure.
The average bond energy (enthalpy) for a C=CC=C double bond is 614 kJ/molkJ/mol and that of a C−CC−C single bond is 348 kJ/molkJ/mol. Estimate the energy needed to break only the ππ bond of the double bond of 2-butene.
Express your answer numerically in joules per molecule.
Chapter 10 Solutions
Introduction to General, Organic and Biochemistry
Ch. 10.3 - Prob. 10.1PCh. 10.4 - Prob. 10.2PCh. 10.4 - Prob. 10.3PCh. 10.4 - Prob. 10.4PCh. 10.4 - Prob. 10.5PCh. 10.4 - Prob. 10.6PCh. 10 - Prob. 10.7PCh. 10 - Prob. 10.8PCh. 10 - 10-9 Is there any difference between vanillin made...Ch. 10 - Prob. 10.10P
Ch. 10 - 10-11 What important experiment did Wohler carry...Ch. 10 - Prob. 10.12PCh. 10 - Prob. 10.13PCh. 10 - Prob. 10.14PCh. 10 - 10-15 How many electrons are in the valence shell...Ch. 10 - 10-16 What is the relationship between the number...Ch. 10 - Prob. 10.17PCh. 10 - Prob. 10.18PCh. 10 - 10-19 Write Lewis structures for these ions. (a)...Ch. 10 - 10-20 Why are the following molecular formulas...Ch. 10 - 10-21 Explain how to use the valence-shell...Ch. 10 - 10-22 Suppose you forget to take into account the...Ch. 10 - Suppose you forget to take into account the...Ch. 10 - 10-24 Use the VSEPR model to predict the bond...Ch. 10 - Prob. 10.25PCh. 10 - Prob. 10.26PCh. 10 - 10-27 What is meant by the term functional group?Ch. 10 - 10-28 List three reasons why functional groups are...Ch. 10 - Prob. 10.29PCh. 10 - Prob. 10.30PCh. 10 - Prob. 10.31PCh. 10 - 10-32 Draw a structural formula for the one...Ch. 10 - 10-33 What is the meaning of the term tertiary (...Ch. 10 - Prob. 10.34PCh. 10 - Draw structural formulas for each of the...Ch. 10 - 10-36 Draw structural formulas for the six ketones...Ch. 10 - 10-37 Draw structural formulas for the eight...Ch. 10 - Prob. 10.38PCh. 10 - 10-39 (Chemical Connections 10A) How was Taxol...Ch. 10 - Prob. 10.40PCh. 10 - Prob. 10.41PCh. 10 - Silicon is immediately below carbon in Group 4A of...Ch. 10 - 10-43 Phosphorus is immediately below nitrogen in...Ch. 10 - Draw the structure for a compound with the...Ch. 10 - 10-45 Draw structural formulas for the eight...Ch. 10 - Prob. 10.46PCh. 10 - 10-47 Which of these covalent bonds are polar, and...Ch. 10 - Of the bonds in Problem 10-47, which is the most...Ch. 10 - Prob. 10.49PCh. 10 - Prob. 10.50PCh. 10 - Following is a structural formula for naphthalene....Ch. 10 - Prob. 10.52PCh. 10 - Prob. 10.53PCh. 10 - Urea, (NH.,)2CO, is used in plastics and in fertil...Ch. 10 - Prob. 10.55PCh. 10 - Prob. 10.56PCh. 10 - Aspirin is prepared by the reaction of salicylic-...Ch. 10 - Following is the structural formula of acetamide....Ch. 10 - Prob. 10.59P
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
- Draw the line-bond structure of oleic acid (cis-9-octadecenoic acid), CH3(CH2)7CH=CH(CH2)7COOH, at physiological pH. You do not need to draw hydrogen atoms attached to carbon atoms.arrow_forwardDraw the bond line structures of the constitutional isomers of C4H10.arrow_forwardDraw the bond line structures for C5H12.arrow_forward
- Draw the Lewis structure of acetic acid, CH3CO2H, clearly indicating all non-bonding pairs of electrons. Even though nitrogen and phosphorus have the same number of valence electrons, nitrogen can only bond to chlorine four times forming NCl4+ but phosphorus can bond with chlorine five times forming PCl5. Explain. Draw all the isomers of C4H9Br, using bond-line formulas. Draw the Lewis structure of the nitrite ion, NO2–, clearly indicating resonance contributors as well as non-bonding pairs of electrons and formal charges, as relevant. Nitromethane is a polar molecule but contains 2 equal polar covalent bonds. Briefly explain why and draw a relevant 3-dimensional structure to show the overall dipole moment of the molecule. Draw all isomers of C6H12O that are aldehydes.arrow_forwardThe carbon–carbon bond length in C2H2 is 1.20 Å, that in C2H4 is 1.34 Å, and that in C2H6 is 1.53 Å. Near which of these values would you predict the bond length of C2 to lie? Is the experimentally observed value, 1.31 Å, consistent with your prediction?arrow_forwardMethyl isocyanate, CH3 -N= C = O, is used in the industrial synthesis of a type of pesticide and herbicide known as a carbamate. As a historical note, an industrial accident in Bhopal, India, in 1984 resulted in leakage of an unknown quantity of this chemical into the air. An estimated 200,000 people were exposed to its vapors, and over 2000 of these people died. Q.) Write a Lewis structure for methyl isocyanate and predict its bond angles. What is the hybridization of its carbonyl carbon? Of its nitrogen atom?arrow_forward
- Consider CH4 and H2O. What is the relationship between the valence electrons in C and O, and the number of hydrogens in the compound ?arrow_forwardEyedrops for dry eyes usually contain a water-soluble polymer called poly(vinyl alcohol), which is based on the unstable organicmolecule vinyl alcohol:arrow_forwardDraw the shapes of the following molecules and ions in 3-dimension. Show clearly any lone pairs of electrons on the central atom, state the number of bond pairs and lone pairs of electrons on the central atom and name the shape of the molecule or ion. (a) CH3+, methyl carbocation (b) HOBr, bromic (I) acid (c) NCl3, nitrogen trichloride Provide everything stated in the instructions for each compound.arrow_forward
- Write the two resonance structures for the pyridinium ion, C5H5NH+.arrow_forwardHydrogen cyanide can be catalytically reduced with hydro-gen to form methylamine. Use Lewis structures and bond ener-gies to determine ΔH°ᵣₓₙ for HCN(g)+2H₂(g)→CH₃NH₂(g)arrow_forwardWhat is the resonance structure(s) of C6H6?arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
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