
(a)
Interpretation:
Synthesis of the given compound is to be shown.
Concept introduction:
The acetic acid is treated with various reagents to form products that contain different

Answer to Problem 21.85P
The synthesis of the given compound is as follows:
Explanation of Solution
The reaction requires converting a carboxylic acid to an acid anhydride, which represents going up the stability ladder. This is difficult to do directly but can be carried out by first producing an acid chloride. The acid chloride and the salt of acetic acid will make the desired anhydride.
The acetic acid is treated with various reagents to form products that contain different functional groups.
(b)
Interpretation:
The synthesis of the given compound is to be shown.
Concept introduction:
The acetic acid is treated with various reagents to form products that contain different functional groups. The new functional groups formed are anhydride, amine, ether, aldehyde, ketone, etc. When carboxylic acid converted to an acid anhydride, the stability ladder going up. When an anhydride reacted with ethanol to formed the ester, the stability ladder going down.

Answer to Problem 21.85P
The synthesis of the given compound is as follows:
Explanation of Solution
The addition of phenol forms the ester under acidic condition, a Fischer esterification. This is a reversible reaction and can be carried out directly because the reactant and product species are on the same rung of the stability ladder.
The acetic acid is treated with various reagents to form products that contain different functional groups.
(c)
Interpretation:
The synthesis of the given compound is to be shown.
Concept introduction:
The acetic acid is treated with various reagents to form products that contain different functional groups. The new functional groups formed are anhydride, amine, ether, aldehyde, ketone, etc. When carboxylic acid converted to an acid anhydride, the stability ladder going up. When an anhydride reacted with ethanol to formed the ester, the stability ladder going down.

Answer to Problem 21.85P
The synthesis of the given compound is as follows,
Explanation of Solution
The reaction of the anhydride from (a) with ethanol makes the ester. This represents going down the stability ladder and is done relatively easily.
The acetic acid is treated with various reagents to form products that contain different functional groups.
(d)
Interpretation:
The synthesis of the given compound is to be shown.
Concept introduction:
The acetic acid is treated with various reagents to form products that contain different functional groups. The new functional groups formed are anhydride, amine, ether, aldehyde, ketone, etc. When carboxylic acid converted to an acid anhydride, the stability ladder going up. When an anhydride reacted with ethanol to formed the ester, the stability ladder going down.

Answer to Problem 21.85P
The synthesis of the given compound is as follows:
Explanation of Solution
The amine can be produced by reducing the corresponding amide. It is difficult to produce the amide directly from acetic acid because the amine that would be required for the nucleophile would deprotonate the carboxylic acid. The amide can be made relatively easily, however, by first converting acetic acid to acetyl chloride and then treating acetyl chloride with the amine.
The acetic acid is treated with various reagents to form products that contain different functional groups.
(e)
Interpretation:
The synthesis of the given compound is to be shown.
Concept introduction:
The acetic acid is treated with various reagents to form products that contain different functional groups. The new functional groups formed are anhydride, amine, ether, aldehyde, ketone, etc. When carboxylic acid converted to an acid anhydride, the stability ladder going up. When an anhydride reacted with ethanol to formed the ester, the stability ladder going down.

Answer to Problem 21.85P
The synthesis of the given compound is as follows,
Explanation of Solution
Reducing the acid to an alcohol, followed by dehydration, leads to the ether. Alternatively, ethanol can be deprotonated by
The acetic acid is treated with various reagents to form products that contain different functional groups.
(f)
Interpretation:
The synthesis of the given compound is to be shown.
Concept introduction:
The acetic acid is treated with various reagents to form products that contain different functional groups. The new functional groups formed are anhydride, amine, ether, aldehyde, ketone, etc. When carboxylic acid converted to an acid anhydride, the stability ladder going up. When an anhydride reacted with ethanol to formed the ester, the stability ladder going down.

Answer to Problem 21.85P
The synthesis of the given compound is as follows,
Explanation of Solution
First, acid is treated with
The acetic acid is treated with various reagents to form products which contain different functional groups.
(g)
Interpretation:
The synthesis of the given compound is to be shown.
Concept introduction:
The acetic acid is treated with various reagents to form products that contain different functional groups. The new functional groups formed are anhydride, amine, ether, aldehyde, ketone, etc. When carboxylic acid converted to an acid anhydride, the stability ladder going up. When an anhydride reacted with ethanol to formed the ester, the stability ladder going down.

Answer to Problem 21.85P
The synthesis of the given compound is as follows,
Explanation of Solution
First, acid is treated with
The acetic acid is treated with various reagents to form products which contain different functional groups.
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Chapter 21 Solutions
Organic Chemistry: Principles and Mechanisms (Second Edition)
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- Please help, this is all the calculations i got!!! I will rate!!!Approx mass of KMnO in vial: 3.464 4 Moss of beaker 3×~0. z Nax200: = 29.9219 Massof weacerv after remosimgain N2C2O4. Need to fill in all the missing blanks. ง ง Approx mass of KMnO4 in vials 3.464 Mass of beaker + 3x ~0-304: 29.9219 2~0.20 Miss of beaker + 2x- 29.7239 Mass of beaker + 1x~0.2g Naz (204 29-5249 Mass of beaver after removing as qa Na₂ C₂O T1 T2 T3 Final Buiet reading Initial butet reading (int)) Hass of NaOr used for Titration -reading (mL) calculation Results: 8.5ml 17mL 27.4mL Oml Om Oml T1 T2 T3 Moles of No CO Moles of KMO used LOF KM. O used Molenty of KMNO Averagem Of KMOWLarrow_forwardDraw the skeletal ("line") structure of 2-hydroxy-4-methylpentanal. Click and drag to start drawing a structure. Xarrow_forwardDetermine whether the following molecule is a hemiacetal, acetal, or neither and select the appropriate box below. Also, highlight the hemiacetal or acetal carbon if there is one. hemiacetal acetal Oneither OHarrow_forward
- What is the missing reactant R in this organic reaction? ་ ་ ་ ་ ་ ་ ་ ་ ་ ་ +R H3O+ • Draw the structure of R in the drawing area below. N • Be sure to use wedge and dash bonds if it's necessary to draw one particular enantiomer. Click and drag to start drawing a structure.arrow_forwardWrite the systematic name of each organic molecule: H structure H OH OH H OH name ☐ OHarrow_forwardDetermine whether each of the following molecules is a hemiacetal, acetal, or neither and select the appropriate box in the table. CH3O OH OH OH hemiacetal acetal neither hemiacetal acetal neither Xarrow_forward
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