
Concept explainers
(a)
Interpretation:
The structural formula of the compound is to be written.
Concept introduction:
To write the structural formula,
(a)

Answer to Problem 56A
Explanation of Solution
The root name ‘pentan’ shows five carbon atoms in the main chain which are single bonded.
The name indicates one methyl group is attached at C-3 and C-1 is carboxylic group (
(b)
Interpretation:
The structural formula of the compound is to be written.
Concept introduction:
To write the structural formula, functional group, number of carbon atoms in the chain is to be identified.
(b)

Answer to Problem 56A
Explanation of Solution
The name ethyl methanoate shows compound contains ester functional group.
Its general formula is
The esters are name by taking alkyl chain from alcoholic part as substituent. Then name of parent chain of
(c)
Interpretation:
The structural formula of the compound is to be written.
Concept introduction:
To write the structural formula, functional group, number of carbon atoms in the chain is to be identified.
(c)

Answer to Problem 56A
Explanation of Solution
The name Methyl benzoate shows compound contains ester functional group.
Its general formula is
The esters are name by taking alkyl chain from alcoholic part as substituent. Then name of parent chain of carboxylic acid is written by removing ‘e’ and adding ‘oate’. So the structure of Methyl benzoate is
(d)
Interpretation:
The structural formula of the compound is to be written.
Concept introduction:
To write the structural formula, functional group, number of carbon atoms in the chain is to be identified.
(d)

Answer to Problem 56A
Explanation of Solution
The root name ‘butan’ shows four carbon atoms in the main chain which are single bonded.
The name indicates one bromo group is attached at C-2 and C-1 is carboxylic group (
(e)
Interpretation:
The structural formula of the compound is to be written.
Concept introduction:
To write the structural formula, functional group, number of carbon atoms in the chain is to be identified.
(e)

Answer to Problem 56A
Explanation of Solution
The root name ‘hexan’ shows six carbon atoms in the main chain which are single bonded.
The name indicates two methyl groups are attached, one at C-2 and other at C-4 and one chloro is attached at C-3 and C-1 is carboxylic group (
Chapter 20 Solutions
World of Chemistry, 3rd edition
- Part B: The line formula for a branched alkane is shown below. a. What is the molecular formula of this compound? Number of C. Number of H b. How many carbon atoms are in the longest chain? c. How many alkyl substituents are attached to this chain?arrow_forward24. What is the major product for the following reaction? Mg J. H.C CH H,C- Then H₂O OH Br C HO E HO H.C CH H.C- CH₂ CH₂ All of these are possiblearrow_forwardstructures. Explain why the major product(s) are formed over the minor product(s) using the Draw the major and product and the complete mechanism for all products with all resonance mechanism/resonance structures of the major and minor products in your explanation. HONO2 H2SO4arrow_forward
- #1 (a). Provide the expected product for the following reaction of A to B by indicating what the product is after step 1 (call this "81") and after step 2 (call this product "B2"). Give a complete mechanism for the transformation of compound A into compound B showing all intermediates, resonance structures, stereochemistry and electron movements 1. Et-MgBr 2. Me-Br B #1 (b). Compound A can be prepared in one step from an alkene starting material. Provide the structure a and the reaction conditions required to convert it to compound A The starting alkenearrow_forwardThe line formula for a branched alkene is shown below. 2 i. What is the molecular formula of this compound? Count number of C and H ii. How many carbon atoms are in the longest chain, ignoring the double bond? iii. What is the longest chain incorporating both carbons of the double bond? iv. How many substituents are on this chain? v. Give the IUPAC name for this compoundarrow_forwardgive the products for each of the followingarrow_forward
- Provide the products and/or reagents for the following transformations. NaOMe HCl/EtOH OH NaOMe CI Show the product for the formation of the ketal given below for the transformation, showing all intermediates and resonance structures would be required to transform the ketal back to the starting ketone and then the mechanism What reagents/conditions HCI EtOH (excess)arrow_forwardMake meta-dibromobenze from nitrobenzene using amine reactions. *see imagearrow_forwardProvide the structure of the expected major and minor (if any) products for each reaction. Clearly indicate stereochemistry where warranted. + + heat heat 이요 HNO3 1. AlCl3 2. H₂O H2SO4 1. AlCl3arrow_forward
- ) Give the mechanism for the acid catalyzed hydrolysis of the following to the corresponding carboxylic acid. Show all intermediates and resonance structures N H+, H2O (excess)arrow_forward# 2. Drow full structures of the organic product expected in each of the following reactions. Draw the appropriate stereoisomer where warranted! Tos Cl O C NaCN PCC శ్రీ CI TSCI Pyridine H₂CrO4 PBrj Pyridine NaCNarrow_forwardPLEASE help. Locate a literature IR spectrum of eugenol. Insert the literature spectrum here: What conclusions can you draw about your clove oil from these IR spectra? I attached my data belowarrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY





