
(a)
Interpretation:
Whether the statement.
The general name of an aliphatic
Concept Introduction:
Alkanoic acid is the IUPAC name of carboxylic acid.
- First choose the longest continuous chain of carbon atoms having carboxyl group known as parent chain.
- The numbering of parent chain should be done in a way that the carboxyl group and substituents get the lowest number.
- The root name of the carbon chain is “oic” acid.
- The appropriate name should be given to every alkyl group and denote its position on the parent chain with the number.
- The alkyl groups are written in alphabetical order.
(b)
Interpretation:
Whether the statement.
A molecule containing two COOH groups is called a dicarboxylic acid is true or false.
Concept Introduction:
Carboxylic acids containing two COOH groups are known as dicarboxylic acid.
(c)
Interpretation:
Whether the statement.
Ethanedioic (oxalic acid) acid is the simplest dicarboxylic acid is true or false.
Concept Introduction:
Oxalic acid contains total two carbon atoms. It’s IUPAC name is ethanedioic acid, here dioic represents the two carboxyl groups.
(d)
Interpretation:
Whether the statement.
3-Methylbutanoic acid is chiral is true or false.
Concept Introduction:
Chiral molecules are those in which there are four different groups attached tetrahedrally.
(e)
Interpretation:
Whether the statement.
The simplest carboxylic acid is methanoic acid (common name: formic acid), HCOOH is true or false.
Concept Introduction:
Formic acid is a carboxylic acid with one carbon.
(f)
Interpretation:
Whether the statement.
Benzoic acid is an
Concept Introduction:
Aromatic carboxylic acid must follow
(g)
Interpretation:
Whether the statement.
Formic acid, which is the common name for HCO2 H, is derived from the word Formica, which is the Latin name for ants is true or false.
Concept Introduction:
Formic acid is a carboxylic acid with one carbon.
(h)
Interpretation:
Whether the statement.
(S)-Lactic acid, CH3 -CHOH-COOH, contains two functional groups: a 20 alcohol and a carboxyl group are true or false.
Concept Introduction:
Lactic acid is 2-hydroxypropanoic acid.

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Chapter 18 Solutions
Bundle: Introduction to General, Organic and Biochemistry, 11th + OWLv2, 4 terms (24 months) Printed Access Card
- 1. Identify the following alkenes as E or Z NH₂ Br 2. Draw the structures based on the IUPAC names (3R,4R)-3-bromo-4-fluoro- 1-hexene (Z)-4-bromo-2-iodo-3-ethyl- 3-heptene تر 3. For the following, predict all possible elimination product(s) and circle the major product. HO H₂SO4 Heat 80 F4 OH H2SO4 Heat 어요 F5 F6 1 A DII 4 F7 F8 F9 % & 5 6 7 * ∞ 8 BAB 3 E R T Y U 9 F D G H J K O A F11 F10arrow_forwardDraw the major product of this reaction. Ignore inorganic byproducts. ○ O 1. H₂O, pyridine 2. neutralizing work-up a N W X 人 Parrow_forward✓ 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_forward
- Draw 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_forwardDraw the major product of this reaction. Ignore inorganic byproducts. N S S HgCl2, H2SO4 く 8 W X Parrow_forward
- tab 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_forwardPart 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_forward
- File 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_forwardCan I please get help with this graph. If you can show exactly where it needs to pass through.arrow_forward
- Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningIntroduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning

