Concept explainers
(a)
Interpretation:
The Lewis structures of
Concept Introduction:
Lewis structures represent covalent bonds and describe valence electrons configuration of atoms. The covalent bonds are depicted by lines, and unshared electron pairs by pairs of dots. The sequence to write Lewis structure of some molecule is given as follows:
- The central atom is identified and various other atoms are arranged around it. This central atom so chosen is often the least electronegative.
- Total valence electrons is estimated for each atoms.
- single bond is first placed between each atom pair.
- The electrons left can be allocated as unshared electron pairs or as multiple bonds around rtegh symbol of elemnt to satisfy the octet (or duplet) for each atom.
- Add charge on overall structure in case of polytatomic cation or anion.
A single bond is always associated with sigma bonds. Molecules that have all atoms connected by sigma bond exclusively are stated to be in
A double bond and carbocation are associated with
A triple bond is always associated with
(b)
Interpretation:
The Lewis structures of
Concept Introduction:
Refer to part (a).
(c)
Interpretation:
The Lewis structures of
Concept Introduction:
Refer to part (a).
Want to see the full answer?
Check out a sample textbook solutionChapter 2 Solutions
CHEMICAL PRINCIPLES PKG W/SAPLING
- In following decomposition reaction:2C3H8(g)⟶ C2H4(g)+ C3H6(g) + CH4(g) + H2(g)For each of the four carbon compounds, do the following: (a) Draw Lewis structure.(b) Predict the geometry about the carbon atom.(c) Determine the hybridization of each type of carbon atom.arrow_forward(a) Complete the Lewis structure for the molecule shown below. How many lone pairs are there? H-C H 1 H (b) Give the hybridizations of the following atoms in the structure: (i) Ca; (ii) Ob (c) Give approximate values of the following bond angles: (i) O a-Ca-Ob; (ii) С a -О b-Сbarrow_forwardPredict the hybridization, geometry, and bond angles for the carbon and nitrogen atoms in acetonitrile (CH3 ¬C ‚ N:).arrow_forward
- Describe the molecular geometry and hybridization of the N, P, or S atoms in each of the following compounds. (a) H3PO4, phosphoric acid, used in cola soft drinks (b) NH4NO3, ammonium nitrate, a fertilizer and explosive (c) S2Cl2, disulfur dichloride, used in vulcanizing rubber (d) K4[O3POPO3], potassium pyrophosphate, an ingredient in some toothpastesarrow_forwardDescribe the molecular geometry and hybridization of the N, P, or S atoms in each of the following compounds.(a) H3PO4, phosphoric acid, used in cola soft drinks(b) NH4NO3, ammonium nitrate, a fertilizer and explosive(c) S2Cl2, disulfur dichloride, used in vulcanizing rubber(d) K4[O3POPO3], potassium pyrophosphate, an ingredient in some toothpastesarrow_forwardButadiene, C4H6, is a planar molecule that has the followingcarbon–carbon bond lengths:(a) Predict the bond angles around each of the carbon atomsand sketch the molecule. (b) From left to right, whatis the hybridization of each carbon atom in butadiene?(c) The middle C¬C bond length in butadiene (1.48 Å) isa little shorter than the average C¬C single bond length(1.54 Å). Does this imply that the middle C¬C bond in butadieneis weaker or stronger than the average C¬C singlebond? (d) Based on your answer for part (c), discuss what additional aspects of bonding in butadiene might supportthe shorter middle C¬C bond.arrow_forward
- (a) Draw Lewis structures for ethane 1C2H62, ethylene1C2H42, and acetylene 1C2H22. (b) What is the hybridizationof the carbon atoms in each molecule? (c) Predict whichmolecules, if any, are planar. (d) How many s and p bondsare there in each molecule?arrow_forwardButadiene, C4H6, is a planar molecule that has the followingcarbon–carbon bond lengths: (a) Predict the bond angles around each of the carbon atoms and sketch the molecule. (b) From left to right, what is the hybridization of each carbon atom in butadiene? (c) The middle C—C bond length in butadiene (1.48 Å) is a little shorter than the average C—C single bond length (1.54 Å). Does this imply that the middle C—C bond in butadiene is weaker or stronger than the average C—C single bond? (d) Based on your answer for part (c), discuss what additional aspects of bonding in butadiene might support the shorter middle C—C bond.arrow_forwardOctocrylene is an ingredient found in topical sunscreens. It is a water-resistant molecule that helps protect skin against harmful UVA and UVB radiation. Octocrylene Please answer the following questions: (a) What is the hybridisation of each nonhydrogen atom? (b) Are there two unique configurations possible about the C=C double bond? Please explain your answer. (c) Which of the two C-C bonds indicated by the arrows would you expect to be shorte.? Please explain your answer.arrow_forward
- Describe the hybrid orbitals used by the carbon atom inN=C-Cl. Predict the geometry of the molecule.arrow_forwardAcetylsalicylic acid, better known as aspirin, has the Lewisstructure (a) What are the approximate values of the bond angles labeled1, 2, and 3? (b) What hybrid orbitals are used about thecentral atom of each of these angles? (c) How many s bondsare in the molecule?arrow_forwardWhen one electron is added to an oxygen molecule, a superoxide ion (Oz) is formed. The addition of two elec- trons gives a peroxide ion (Oź ). Removal of an electron from O, leads to Ož. (a) Construct the correlation diagram for Oz. (b) Give the valence electron configuration for each of the following species: Ož, O2, 0z, 03 . (c) Give the bond order of each species. (d) Predict which species are paramagnetic. (e) Predict the order of increasing bond dissociation energy among the species.arrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY