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Concept explainers
a) The H-Cl bond length is 136pm. What would be the dipole moment of H-Cl be if the molecule were 100% ionic, H+Cl-?
Interpretation:
Assuming H-Cl to be 100% ionic its dipole moment is to be calculated. Its bond length is given as 136pm.
Concept introduction:
Dipole moment is defined as, µ=Qxr
Where, Q=Magnitude of the charge developed at either end of the dipole.
R=The distance between the charges
It is expressed in Debyes (D). 1 D=3.336x10-30C.m
To determine:
The dipole moment of H-Cl assuming it to be 100% ionic. Its bond length is given as 136pm.
b) The actual dipole moment of H-Cl is 1.08 D. What is the percent ionic character of the H-Cl bond.
Interpretation:
Actual dipole moment of H-Cl is given as 1.08 D. Its percent ionic character is to be calculated.
Concept introduction:
Assuming H-Cl to be 100% ionic and knowing the bond length, the dipole moment of H-Cl can be calculated. From the calculated value and the actual value of dipole moments the percent of ionic character of H-Cl can be determined.
To determine:
The percent ionic character of the H-Cl bond, if its actual dipole moment is 1.08 D.
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Chapter 2 Solutions
OWLv2 with Student Solutions Manual eBook, 4 terms (24 months) Printed Access Card for McMurry's Organic Chemistry, 9th
- IV. Show the detailed synthesis strategy for the following compounds. a. CH3CH2CH2CH2Br CH3CH2CCH2CH2CH3arrow_forwardDo the electrons on the OH participate in resonance with the ring through a p orbital? How many pi electrons are in the ring, 4 (from the two double bonds) or 6 (including the electrons on the O)?arrow_forwardPredict and draw the product of the following organic reaction:arrow_forward
- Nonearrow_forwardRedraw the molecule below as a skeletal ("line") structure. Be sure to use wedge and dash bonds if necessary to accurately represent the direction of the bonds to ring substituents. Cl. Br Click and drag to start drawing a structure. : ☐ ☑ Parrow_forwardK m Choose the best reagents to complete the following reaction. L ZI 0 Problem 4 of 11 A 1. NaOH 2. CH3CH2CH2NH2 1. HCI B OH 2. CH3CH2CH2NH2 DII F1 F2 F3 F4 F5 A F6 C CH3CH2CH2NH2 1. SOCl2 D 2. CH3CH2CH2NH2 1. CH3CH2CH2NH2 E 2. SOCl2 Done PrtScn Home End FA FQ 510 * PgUp M Submit PgDn F11arrow_forward
- given cler asnwerarrow_forwardAdd curved arrows to the reactants in this reaction. A double-barbed curved arrow is used to represent the movement of a pair of electrons. Draw curved arrows. : 0: si H : OH :: H―0: Harrow_forwardConsider this step in a radical reaction: Br N O hv What type of step is this? Check all that apply. Draw the products of the step on the right-hand side of the drawing area below. If more than one set of products is possible, draw any set. Also, draw the mechanism arrows on the left-hand side of the drawing area to show how this happens. O primary Otermination O initialization O electrophilic O none of the above × ☑arrow_forward
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