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Concept explainers
(a)
Interpretation:
The alcohol and the acid chloride that combines to make the given ester are to be stated.
Concept introduction:
An alcohol and an acid chloride mix together and form an ester with removal of hydrogen chloride. To neutralize the hydrogen chloride (side product), pyridine is used as a catalyst.
(b)
Interpretation:
The alcohol and the acid chloride that combines to make the given ester are to be stated.
Concept introduction:
An alcohol and an acid chloride mix together and form an ester with removal of hydrogen chloride. To neutralize the hydrogen chloride (side product), pyridine is used as a catalyst.
(c)
Interpretation:
The alcohol and the acid chloride that combines to make the given ester are to be stated.
Concept introduction:
An alcohol and an acid chloride mix together and form an ester with removal of hydrogen chloride. To neutralize the hydrogen chloride (side product), pyridine is used as a catalyst.
(d)
Interpretation:
The alcohol and the acid chloride that combines to make the given ester are to be stated.
Concept introduction:
An alcohol and an acid chloride mix together and form an ester with removal of hydrogen chloride. To neutralize the hydrogen chloride (side product), pyridine is used as a catalyst.
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Chapter 11 Solutions
Organic Chemistry (9th Edition)
- 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
- Nonearrow_forwardCan I get a drawing of what is happening with the orbitals (particularly the p orbital) on the O in the OH group? Is the p orbital on the O involved in the ring resonance? Why or why not?arrow_forward1) How many monochlorination products-including stereochemistry- are there for the molecule below:arrow_forward
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