
(a)
To determine: The formation of given ether in good yield by condensation of the corresponding alcohol and the alternative method for the ether that cannot be prepared by the condensation of the alcohols.
Interpretation: The formation of given ether in good yield by condensation of the corresponding alcohol and the alternative method for the ether that cannot be prepared by the condensation of the alcohols is to be identified.
Concept introduction: In a condensation reaction, two molecules join together to form a large molecule with the removal of small molecule such as water.
(b)
To determine: The formation of the given ether in good yield by condensation of the corresponding alcohol and the alternative method for the ether that cannot be prepared by the condensation of the alcohols.
Interpretation: The formation of given ether in good yield by condensation of the corresponding alcohol and the alternative method for the ether that cannot be prepared by the condensation of the alcohols is to be identified.
Concept introduction: The reaction of an alkoxide ion with
(c)
To determine: The formation of given ether in good yield by condensation of the corresponding alcohol and the alternative method for the ether that cannot be prepared by the condensation of the alcohols.
Interpretation: The formation of given ether in good yield by condensation of the corresponding alcohol and the alternative method for the ether that cannot be prepared by the condensation of the alcohols is to be identified.
Concept introduction: In alkoxymercuration-demercuration, ether is produced when

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Chapter 14 Solutions
Organic Chemistry (9th Edition)
- Draw the complete mechanism for the acid-catalyzed hydration of this alkene. esc 田 Explanation Check 1 888 Q A slock Add/Remove step Q F4 F5 F6 A བྲA F7 $ % 5 @ 4 2 3 & 6 87 Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Ce W E R T Y U S D LL G H IK DD 요 F8 F9 F10 F1 * ( 8 9 0 O P J K L Z X C V B N M H He commandarrow_forwardExplanation Check F1 H₂O H₂ Pd 1) MCPBA 2) H3O+ 1) Hg(OAc)2, H₂O 2) NaBH4 OH CI OH OH OH hydration halohydrin formation addition halogenation hydrogenation inhalation hydrogenation hydration ☐ halohydrin formation addition halogenation formation chelation hydrogenation halohydrin formation substitution hydration halogenation addition Ohalohydrin formation subtraction halogenation addition hydrogenation hydration F2 80 F3 σ F4 F5 F6 1 ! 2 # 3 $ 4 % 05 Q W & Å © 2025 McGraw Hill LLC. All Rights Reserved. F7 F8 ( 6 7 8 9 LU E R T Y U A F9arrow_forwardShow the mechanism steps to obtain the lowerenergy intermediate: *see imagearrow_forward
- Soap is made by the previous reaction *see image. The main difference between one soap and another soap isthe length (number of carbons) of the carboxylic acid. However, if a soap irritates your skin, they mostlikely used too much lye.Detergents have the same chemical structure as soaps except for the functional group. Detergentshave sulfate (R-SO4H) and phosphate (R-PO4H2) functional groups. Draw the above carboxylic acidcarbon chain but as the two variants of detergents. *see imagearrow_forwardWhat are the reactions or reagents used? *see imagearrow_forwardWhat are the reactions or reagents used? *see imagearrow_forward
- Provide the mechanism for this transformation: *see imagearrow_forwardAssign all the signals individually (please assign the red, green and blue)arrow_forwardThe two pKa values of oxalic acid are 1.25 and 3.81. Why are they not the same value? Show the protontransfer as part of your explanation. *see imagearrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
