Student Study Guide and Solutions Manual for Brown/Iverson/Anslyn/Foote's Organic Chemistry, 8th Edition
8th Edition
ISBN: 9781305864504
Author: Brent L. Iverson, Sheila Iverson
Publisher: Cengage Learning
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Textbook Question
Chapter 5, Problem 5.11P
The structure of 1,2-propadiene (allene) is shown to the right.
- (a) Predict all approximate bond angles in this molecule.
- (b) State the orbital hybridization of each carbon.
- (c) Explain the three-dimensional geometry of allene in terms of the orbitals used.
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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 toothpastes
Chapter 5 Solutions
Student Study Guide and Solutions Manual for Brown/Iverson/Anslyn/Foote's Organic Chemistry, 8th Edition
Ch. 5.1 - Calculate the index of hydrogen deficiency for...Ch. 5.1 - Prob. 5.2PCh. 5.2 - Write the IUPAC name of each alkene. (a) (b)Ch. 5.2 - Prob. 5.4PCh. 5.2 - Prob. 5.5PCh. 5.2 - Prob. 5.6PCh. 5.2 - Prob. 5.7PCh. 5.2 - Prob. 5.8PCh. 5 - Predict all approximate bond angles about each...Ch. 5 - Prob. 5.10P
Ch. 5 - The structure of 1,2-propadiene (allene) is shown...Ch. 5 - Prob. 5.12PCh. 5 - Draw structural formulas for these alkenes. (a)...Ch. 5 - Name these alkenes and cycloalkenes.Ch. 5 - Prob. 5.15PCh. 5 - Prob. 5.16PCh. 5 - Prob. 5.17PCh. 5 - For each molecule that shows cis, trans isomerism,...Ch. 5 - -Ocimene, a triene found in the fragrance of...Ch. 5 - Prob. 5.20PCh. 5 - Prob. 5.21PCh. 5 - Prob. 5.22PCh. 5 - Prob. 5.23PCh. 5 - Prob. 5.24PCh. 5 - Measure the CH3,CH3 distance in the...Ch. 5 - Prob. 5.26PCh. 5 - Measure the CCC and CCH bond angles in the...Ch. 5 - Prob. 5.28PCh. 5 - Prob. 5.29PCh. 5 - Prob. 5.30PCh. 5 - Prob. 5.31PCh. 5 - Prob. 5.32PCh. 5 - Prob. 5.33PCh. 5 - Pyrethrin II and pyrethrosin are two natural...Ch. 5 - Prob. 5.35PCh. 5 - Prob. 5.36PCh. 5 - Bromine adds to cis- and trans-2-butene to give...
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- 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_forwardIdentify any carbon atoms that change hybridization and the change in hybridization during the reactions in (a) 2-butene reacts with chlorine.(b) benzene burns in air.arrow_forwardFor each statement, indicate whether it is true or false. (a) The greater the orbital overlap in a bond, the weaker the bond. [b] The greater the orbital overlap in a bond, the shorter the bond. [c] To create a hybrid orbital, you could use the s orbital on one atom with a p orbital on another atom. [d] Nonbonding electron pairs cannot occupy a hybrid orbital.arrow_forward
- (a) Describe the hybridization of the central atom of a molecule with a see-saw shape. (b) Describe the hybridization of the central atom of a molecule with a trigonal planar shape. (c) Describe the hybridization of the central atom of a molecule with a trigonal bipyramidal shape.arrow_forwardDraw a Lewis electron dot diagram for each of the follow- ing molecules and ions. Formulate the hybridization for the central atom in each case and give the molecular geometry. (a) BF3 (b) BH4- (c) PH3 (d) CS2 (e) CH3+arrow_forwardOrganic compounds (a) A simple molecule with alternating single and double bonds is buta-1,3-diene. (i) Draw its skeletal structure. (ii) Write its molecular formula and empirical formula. (iii) How many carbon atoms have sp2 hybridization in buta-1,3-diene?arrow_forward
- (a) Find the angle u between adjacent nearest-neighbor bonds in the silicon lattice. Recall that each silicon atom is bonded to four of its nearest neighbors.The four neighbors form a regular tetrahedron— a pyramid whose sides and base are equilateral triangles. (b) Find the bond length, given that the atoms at the corners of the tetrahedron are 388 pm apart.arrow_forward(a) State the hybrid orbitals for C1,C2,O1 and O2 (b) state the number of π bonds present (c) State teh number of C atoms with sp2 hybridization.arrow_forward(a) Sketch the molecular orbitals of the H2- ion and draw itsenergy-level diagram. (b) Write the electron configuration ofthe ion in terms of its MOs. (c) Calculate the bond order inH2-. (d) Suppose that the ion is excited by light, so that anelectron moves from a lower-energy to a higher-energy molecularorbital. Would you expect the excited-state H2- ion to bestable? (e) Which of the following statements about part (d) is correct: (i) The light excites an electron from a bonding orbitalto an antibonding orbital, (ii) The light excites an electronfrom an antibonding orbital to a bonding orbital, or (iii)In the excited state there are more bonding electrons thanantibonding electrons?arrow_forward
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