(a)
Interpretation:
A wedge-bond structure of chloroform has to be drawn; the most effective direction of iodide ion
Concept Introduction:
Molecular geometry: The term molecular geometry refers to the 3-dimensional shape of the molecule by which the molecule is occupying in space with all its surrounding atoms or ions and/or lone pair of electrons.
Hybridization is the phenomenon of intermixing of the atomic orbitals of different energy that results in the formation of a new set of hybrid orbitals which have equivalent energies. The various types of atomic orbitals are: s, p, and d orbitals. Types of hybridization that involves s, p and d orbitals are
(b)
Interpretation:
A wedge bond structure of product has to be explained.
Concept Introduction:
Molecular geometry: The term molecular geometry refers to the 3-dimensional shape of the molecule by which the molecule is occupying in space with all its surrounding atoms or ions and/or lone pair of electrons.
Hybridization is the phenomenon of intermixing of the atomic orbitals of different energy that results in the formation of a new set of hybrid orbitals which have equivalent energies. The various types of atomic orbitals are: s, p, and d orbitals. Types of hybridization that involves s, p and d orbitals are
(c)
Interpretation:
The given structure possessing no optical activity has to be explained.
Concept Introduction:
Optical isomerism of substituted
Optical isomers are non-superimposable mirror images. The carbon atom attached with four different substituents or group of atoms is known as chiral centre asymmetric carbon.
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Chapter 16 Solutions
CHEMISTRY:MOLEC NAT PRINT COMPANION
- Using line angle formulas, draw thestructures of and name four alkanes that have total of 7carbons, one of which is tertiary.Please explain this in detail and can you also explain how to approach a similar problem like this as well?arrow_forwardUsing dashed line wedge projections drawthe indicated compounds and indicate whether thecompound you have drawn is R or S.(a) The two enantiomers of 2-chlorobutane. Can you please explain your steps and how you would approach a similar problem. Thank you!arrow_forward5) There are no lone pairs shown in the structure below. Please add in all lone pairs and then give the hybridization scheme for the compound. (8) 10,11 7) 1.2.3 H 4 | 14 8) COC 12 13 H 16 15 H7 9) - 5.6 C 8 H 10) H 1). 2) 3)_ 11) 12) 13) 4)_ 14) 5) 15) 16) 6)arrow_forward
- The sum of the numbers in the name of isA. 11; B. 13; C. 10; D. 12; E. none of the other answers iscorrect. I believe the awnser should be E to this problem but the solution to this problem is D 12. I'm honestly unsure how that's the solution. If you can please explain the steps to this type of problem and how to approach a problem like this it would be greatly appreciated!arrow_forwardConsider the following data for phosphorus: g atomic mass 30.974 mol electronegativity 2.19 kJ electron affinity 72. mol kJ ionization energy 1011.8 mol kJ heat of fusion 0.64 mol You may find additional useful data in the ALEKS Data tab. Does the following reaction absorb or release energy? 2+ + (1) P (g) + e → P (g) Is it possible to calculate the amount of energy absorbed or released by reaction (1) using only the data above? If you answered yes to the previous question, enter the amount of energy absorbed or released by reaction (1): Does the following reaction absorb or release energy? 00 release absorb Can't be decided with the data given. yes no ☐ kJ/mol (²) P* (8) + + + e →>> P (g) Is it possible to calculate the amount of energy absorbed or released by reaction (2) using only the data above? If you answered yes to the previous question, enter the amount of energy absorbed or released by reaction (2): ☐ release absorb Can't be decided with the data given. yes no kJ/mol аarrow_forwardThe number of hydrogens in an alkyne that has a main chain of 14carbons to which are attached a cyclobutyl ring, a benzene ring, an–OH group, and a Br is A. 34; B. 35; C. 36; D. 24; E. 43arrow_forward
- Hello! I have a 500 Hz H-NMR for 1,5-bis-(4-methoxyphenyl)-penta-1,4-dien-3-one. I need to label the signals with the corresponding H's. Then, find out if the two alkenes are cis or trans by calculating the J values. I believe that I have the H-NMR labeled correctly, but not sure if I got the J values correct to determine if the two alkenes in the compound will make the compound cis or trans.arrow_forwardWhat is the only possible H-Sb-H bond angle in SbH3?arrow_forwardpls helparrow_forward
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