
Concept explainers
(a)
Interpretation:
Physical state at room temperature for oxalic acid has to be given.
Concept Introduction:
Physical property of
(b)
Interpretation:
Physical state at room temperature for decanoic acid has to be given.
Concept Introduction:
Physical property of carboxylic acid is decided by the carbon chain and the functional group. Carboxylic acids are highly polar, as the carboxyl group is more polar. Due to this polar nature, the melting and boiling point are very high. Monocarboxylic acids that are unsubstituted which contains up to nine carbon atoms are present in liquid state. They have very sharp odor. Monocarboxylic acids that have more than ten carbon atoms in an unbranched fashion are waxy solids. They do not have any odor because of low volatility. Similar to this, dicarboxylic acids and aromatic carboxylic acids do not have any odor and they are solids.
(c)
Interpretation:
Physical state at room temperature for hexanoic acid has to be given.
Concept Introduction:
Physical property of carboxylic acid is decided by the carbon chain and the functional group. Carboxylic acids are highly polar, as the carboxyl group is more polar. Due to this polar nature, the melting and boiling point are very high. Monocarboxylic acids that are unsubstituted which contains up to nine carbon atoms are present in liquid state. They have very sharp odor. Monocarboxylic acids that have more than ten carbon atoms in an unbranched fashion are waxy solids. They do not have any odor because of low volatility. Similar to this, dicarboxylic acids and aromatic carboxylic acids do not have any odor and they are solids.
(d)
Interpretation:
Physical state at room temperature for benzoic acid has to be given.
Concept Introduction:
Physical property of carboxylic acid is decided by the carbon chain and the functional group. Carboxylic acids are highly polar, as the carboxyl group is more polar. Due to this polar nature, the melting and boiling point are very high. Monocarboxylic acids that are unsubstituted which contains up to nine carbon atoms are present in liquid state. They have very sharp odor. Monocarboxylic acids that have more than ten carbon atoms in an unbranched fashion are waxy solids. They do not have any odor because of low volatility. Similar to this, dicarboxylic acids and aromatic carboxylic acids do not have any odor and they are solids.

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Chapter 16 Solutions
Bundle: General, Organic, and Biological Chemistry, 7th + OWLv2 Quick Prep for General Chemistry, 4 terms (24 months) Printed Access Card
- ✓ Check the box under each molecule that has a total of five ẞ hydrogens. If none of the molecules fit this description, check the box underneath the table. tab OH CI 0 Br xx Br None of these molecules have a total of five ẞ hydrogens. esc Explanation Check caps lock shift 1 fn control 02 F2 W Q A N #3 S 80 F3 E $ t 01 205 % 5 F5 & 7 © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility FT * 8 R T Y U כ F6 9 FIG F11 F D G H J K L C X V B < N M H option command P H + F12 commandarrow_forwardDraw the major product of this reaction. Ignore inorganic byproducts and the carboxylic acid side product. O 1. CHзMgBr (excess) 2. H₂O ✓ W X 人arrow_forwardIf cyclopentyl acetaldehyde reacts with NaOH, state the product (formula).arrow_forward
- Draw the major product of this reaction. Ignore inorganic byproducts. N S S HgCl2, H2SO4 く 8 W X Parrow_forwardtab esc く Drawing the After running various experiments, you determine that the mechanism for the following reaction occurs in a step-wise fashion. Br + OH + Using this information, draw the correct mechanism in the space below. 1 Explanation Check F2 F1 @2 Q W A os lock control option T S # 3 80 F3 Br $ 4 0105 % OH2 + Br Add/Remove step X C F5 F6 6 R E T Y 29 & 7 F D G H Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Ce A F7 DII F8 C Ո 8 * 9 4 F10 F C J K L C V Z X B N M H command P ge Coarrow_forwardIndicate compound A that must react with ethylbenzene to obtain 4-ethylbenzene-1-sulfonic acid. 3-bromo-4-ethylbenzene-1-sulfonic acid.arrow_forward
- Part 1 of 2 Draw the structure of A, the minor E1 product of the reaction. esc I Skip Part Check H₂O, D 2 A + Click and drag to start drawing a structure. -0- F1 F2 1 2 # 3 Q A 80 F3 W E S D F4 $ 4 % 5 F5 ㅇ F6 R T Y F G X 5 & 7 + Save 2025 McGraw Hill LLC. All Rights Reserved. DII F7 F8 H * C 80 J Z X C V B N 4 F9 6arrow_forwardFile Preview The following is a total synthesis of the pheromone of the western pine beetle. Such syntheses are interesting both because of the organic chemistry, and because of the possibility of using species specific insecticides, rather than broad band insecticides. Provide the reagents for each step. There is some chemistry from our most recent chapter in this synthesis, but other steps are review from earlier chapters. (8 points) COOEt COOEt A C COOEt COOEt COOH B OH OTS CN D E See the last homework set F for assistance on this one. H+, H₂O G OH OH The last step is just nucleophilic addition reactions, taking the ketone to an acetal, intramolecularly. But it is hard to visualize the three dimensional shape as it occurs. Frontalin, pheromone of the western pine beetlearrow_forwardFor the reaction below: 1. Draw all reasonable elimination products to the right of the arrow. 2. In the box below the reaction, redraw any product you expect to be a major product. C Major Product: Check + ◎ + X ง © Cl I F2 80 F3 I σ F4 I F5 NaOH Click and drawing F6 A 2025 McGraw Hill LLC. All Rights E F7 F8 $ # % & 2 3 4 5 6 7 8 Q W E R T Y U A S D F G H Jarrow_forward
- Can I please get help with this graph. If you can show exactly where it needs to pass through.arrow_forwardN Draw the major product of this reaction. Ignore inorganic byproducts. D 1. H₂O, pyridine 2. neutralizing work-up V P W X DE CO e C Larrow_forwardDraw the major product of this reaction. Ignore inorganic byproducts. N O' 1. H2O, pyridine 2. neutralizing work-up く 8 W aarrow_forward
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