(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 17 Solutions
Introduction to General, Organic and Biochemistry
- curved arrows are used to illustrate the flow of electrons. using the provided starting and product structures, draw the cured electron-pushing arrows for thw following reaction or mechanistic steps. be sure to account for all bond-breaking and bond making stepsarrow_forwardUsing the graphs could you help me explain the answers. I assumed that both graphs are proportional to the inverse of time, I think. Could you please help me.arrow_forwardSynthesis of Dibenzalacetone [References] Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone below. Question 1 1 pt Question 2 1 pt Question 3 1 pt H Question 4 1 pt Question 5 1 pt Question 6 1 pt Question 7 1pt Question 8 1 pt Progress: 7/8 items Que Feb 24 at You do not have to consider stereochemistry. . Draw the enolate ion in its carbanion form. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. ⚫ Separate multiple reactants using the + sign from the drop-down menu. ? 4arrow_forward
- Shown below is the mechanism presented for the formation of biasplatin in reference 1 from the Background and Experiment document. The amounts used of each reactant are shown. Either draw or describe a better alternative to this mechanism. (Note that the first step represents two steps combined and the proton loss is not even shown; fixing these is not the desired improvement.) (Hints: The first step is correct, the second step is not; and the amount of the anhydride is in large excess to serve a purpose.)arrow_forwardHi I need help on the question provided in the image.arrow_forwardDraw a reasonable mechanism for the following reaction:arrow_forward
- Draw the mechanism for the following reaction: CH3 CH3 Et-OH Et Edit the reaction by drawing all steps in the appropriate boxes and connecting them with reaction arrows. Add charges where needed. Electron-flow arrows should start on the electron(s) of an atom or a bond and should end on an atom, bond, or location where a new bond should be created. H± EXP. L CONT. י Α [1] осн CH3 а CH3 :Ö Et H 0 N о S 0 Br Et-ÖH | P LL Farrow_forward20.00 mL of 0.150 M NaOH is titrated with 37.75 mL of HCl. What is the molarity of the HCl?arrow_forward20.00 mL of 0.025 M HCl is titrated with 0.035 M KOH. What volume of KOH is needed?arrow_forward
- 20.00 mL of 0.150 M NaOH is titrated with 37.75 mL of HCl. What is the molarity of the HCl?arrow_forward20.00 mL of 0.025 M HCl is titrated with 0.035 M KOH. What volume of KOH is needed?arrow_forward20.00 mL of 0.150 M HCl is titrated with 37.75 mL of NaOH. What is the molarity of the NaOH?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

