
Concept explainers
(a)
Interpretation:
The systematic name of the given compound should be checked and has to be corrected if the given name is wrong.
Concept Introduction:
- The first step is to find out the parent chain of the hydrocarbon. Parent chain should contain maximum number of multiple bonds, maximum number of substituents of the
functional group which is used as main suffix. - Other functional group, if any, should be identified and name it as prefix.
- Numbering should be done in such a way that to get the lowest number for suffix functional group, multiple bonds.
- The punctuation used to separate numbers is commas and hyphen is used to separate a number and alphabet.
- If the ‘ane’ ending of the
alkane is replaced by ‘yne’ ending, the name of alkyne is obtained. - Select the longest chain which contain the triple bond in such a way to get lowest value for the functional group.
- Two types of
alkynes will be there according to the position of triple bond. Terminal alkyne is the one which contain triple bond at the end of the chain and internal alkyne is the one which contain triple bond not at the end but present in any other positions in the chain. - When the counting is done from either sides of triple bond in a compound which contain same number for the functional group suffix, the correct name will be the one which have lowest substituent number. In the case of more than one substituent, alphabetical order should be followed.
Skeletal structure: When the atoms bonded in a compound is drawn in a series it can be called as a skeletal structure. In the skeletal structure, we can show the branches, chains, rings or any other hetero atom other than carbon or hydrogen.
Condensed structure: In the condensed structure, atoms or group of atoms are expressed in a line. But it does not contain any vertical bonds and also the horizontal single bonds.
(b)
Interpretation:
The systematic name of the given compound should be checked and has to be corrected if the given name is wrong.
Concept Introduction:
IUPAC NOMENCLATURE RULES:
- The first step is to find out the parent chain of the hydrocarbon. Parent chain should contain maximum number of multiple bonds, maximum number of substituents of the functional group which is used as main suffix.
- Other functional group, if any, should be identified and name it as prefix.
- Numbering should be done in such a way that to get the lowest number for suffix functional group, multiple bonds.
- The punctuation used to separate numbers is commas and hyphen is used to separate a number and alphabet.
- If the ‘ane’ ending of the alkane is replaced by ‘yne’ ending, the name of alkyne is obtained.
- Select the longest chain which contain the triple bond in such a way to get lowest value for the functional group.
- Two types of alkynes will be there according to the position of triple bond. Terminal alkyne is the one which contain triple bond at the end of the chain and internal alkyne is the one which contain triple bond not at the end but present in any other positions in the chain.
- When the counting is done from either sides of triple bond in a compound which contain same number for the functional group suffix, the correct name will be the one which have lowest substituent number. In the case of more than one substituent, alphabetical order should be followed.
Skeletal structure: When the atoms bonded in a compound is drawn in a series it can be called as a skeletal structure. In the skeletal structure, we can show the branches, chains, rings or any other hetero atom other than carbon or hydrogen.
Condensed structure: In the condensed structure, atoms or group of atoms are expressed in a line. But it does not contain any vertical bonds and also the horizontal single bonds.
(c)
Interpretation:
The systematic name of the given compound should be checked and has to be corrected if the given name is wrong.
Concept Introduction:
IUPAC NOMENCLATURE RULES:
- The first step is to find out the parent chain of the hydrocarbon. Parent chain should contain maximum number of multiple bonds, maximum number of substituents of the functional group which is used as main suffix.
- Other functional group, if any, should be identified and name it as prefix.
- Numbering should be done in such a way that to get the lowest number for suffix functional group, multiple bonds.
- The punctuation used to separate numbers is commas and hyphen is used to separate a number and alphabet.
- If the ‘ane’ ending of the alkane is replaced by ‘yne’ ending, the name of alkyne is obtained.
- Select the longest chain which contain the triple bond in such a way to get lowest value for the functional group.
- Two types of alkynes will be there according to the position of triple bond. Terminal alkyne is the one which contain triple bond at the end of the chain and internal alkyne is the one which contain triple bond not at the end but present in any other positions in the chain.
- When the counting is done from either sides of triple bond in a compound which contain same number for the functional group suffix, the correct name will be the one which have lowest substituent number. In the case of more than one substituent, alphabetical order should be followed.
Skeletal structure: When the atoms bonded in a compound is drawn in a series it can be called as a skeletal structure. In the skeletal structure, we can show the branches, chains, rings or any other hetero atom other than carbon or hydrogen.
Condensed structure: In the condensed structure, atoms or group of atoms are expressed in a line. But it does not contain any vertical bonds and also the horizontal single bonds.
(d)
Interpretation:
The systematic name of the given compound should be checked and has to be corrected if the given name is wrong.
Concept Introduction:
IUPAC NOMENCLATURE RULES:
- The first step is to find out the parent chain of the hydrocarbon. Parent chain should contain maximum number of multiple bonds, maximum number of substituents of the functional group which is used as main suffix.
- Other functional group, if any, should be identified and name it as prefix.
- Numbering should be done in such a way that to get the lowest number for suffix functional group, multiple bonds.
- The punctuation used to separate numbers is commas and hyphen is used to separate a number and alphabet.
- If the ‘ane’ ending of the alkane is replaced by ‘yne’ ending, the name of alkyne is obtained.
- Select the longest chain which contain the triple bond in such a way to get lowest value for the functional group.
- Two types of alkynes will be there according to the position of triple bond. Terminal alkyne is the one which contain triple bond at the end of the chain and internal alkyne is the one which contain triple bond not at the end but present in any other positions in the chain.
- When the counting is done from either sides of triple bond in a compound which contain same number for the functional group suffix, the correct name will be the one which have lowest substituent number. In the case of more than one substituent, alphabetical order should be followed.
Skeletal structure: When the atoms bonded in a compound is drawn in a series it can be called as a skeletal structure. In the skeletal structure, we can show the branches, chains, rings or any other hetero atom other than carbon or hydrogen.
Condensed structure: In the condensed structure, atoms or group of atoms are expressed in a line. But it does not contain any vertical bonds and also the horizontal single bonds.
(e)
Interpretation:
The systematic name of the given compound should be checked and has to be corrected if the given name is wrong.
Concept Introduction:
IUPAC NOMENCLATURE RULES:
- The first step is to find out the parent chain of the hydrocarbon. Parent chain should contain maximum number of multiple bonds, maximum number of substituents of the functional group which is used as main suffix.
- Other functional group, if any, should be identified and name it as prefix.
- Numbering should be done in such a way that to get the lowest number for suffix functional group, multiple bonds.
- The punctuation used to separate numbers is commas and hyphen is used to separate a number and alphabet.
- If the ‘ane’ ending of the alkane is replaced by ‘yne’ ending, the name of alkyne is obtained.
- Select the longest chain which contain the triple bond in such a way to get lowest value for the functional group.
- Two types of alkynes will be there according to the position of triple bond. Terminal alkyne is the one which contain triple bond at the end of the chain and internal alkyne is the one which contain triple bond not at the end but present in any other positions in the chain.
- When the counting is done from either sides of triple bond in a compound which contain same number for the functional group suffix, the correct name will be the one which have lowest substituent number. In the case of more than one substituent, alphabetical order should be followed.
Skeletal structure: When the atoms bonded in a compound is drawn in a series it can be called as a skeletal structure. In the skeletal structure, we can show the branches, chains, rings or any other hetero atom other than carbon or hydrogen.
Condensed structure: In the condensed structure, atoms or group of atoms are expressed in a line. But it does not contain any vertical bonds and also the horizontal single bonds.
(f)
Interpretation:
The systematic name of the given compound should be checked and has to be corrected if the given name is wrong.
Concept Introduction:
IUPAC NOMENCLATURE RULES:
- The first step is to find out the parent chain of the hydrocarbon. Parent chain should contain maximum number of multiple bonds, maximum number of substituents of the functional group which is used as main suffix.
- Other functional group, if any, should be identified and name it as prefix.
- Numbering should be done in such a way that to get the lowest number for suffix functional group, multiple bonds.
- The punctuation used to separate numbers is commas and hyphen is used to separate a number and alphabet.
- If the ‘ane’ ending of the alkane is replaced by ‘yne’ ending, the name of alkyne is obtained.
- Select the longest chain which contain the triple bond in such a way to get lowest value for the functional group.
- Two types of alkynes will be there according to the position of triple bond. Terminal alkyne is the one which contain triple bond at the end of the chain and internal alkyne is the one which contain triple bond not at the end but present in any other positions in the chain.
- When the counting is done from either sides of triple bond in a compound which contain same number for the functional group suffix, the correct name will be the one which have lowest substituent number. In the case of more than one substituent, alphabetical order should be followed.
Skeletal structure: When the atoms bonded in a compound is drawn in a series it can be called as a skeletal structure. In the skeletal structure, we can show the branches, chains, rings or any other hetero atom other than carbon or hydrogen.
Condensed structure: In the condensed structure, atoms or group of atoms are expressed in a line. But it does not contain any vertical bonds and also the horizontal single bonds.

Want to see the full answer?
Check out a sample textbook solution
Chapter 7 Solutions
Organic Chemistry (8th Edition)
- Provide steps and explanation please.arrow_forwardDraw a structural formula for the major product of the acid-base reaction shown. H 0 N + HCI (1 mole) CH3 N' (1 mole) CH3 You do not have to consider stereochemistry. ● • Do not include counter-ions, e.g., Na+, I, in your answer. . In those cases in which there are two reactants, draw only the product from 989 CH3 344 ? [Farrow_forwardQuestion 15 What is the major neutral organic product for the following sequence? 1. POCI₂ pyridine ? 2. OsO4 OH 3. NaHSO Major Organic Product ✓ OH OH 'OH OH 'OH 'CIarrow_forward
- Could you please solve the first problem in this way and present it similarly but color-coded or step by step so I can understand it better? Thank you!arrow_forwardCould you please solve the first problem in this way and present it similarly but color-coded or step by step so I can understand it better? Thank you!arrow_forwardCould you please solve the first problem in this way and present it similarly but (color-coded) and step by step so I can understand it better? Thank you! I want to see what they are doingarrow_forward
- Can you please help mne with this problem. Im a visual person, so can you redraw it, potentislly color code and then as well explain it. I know im given CO2 use that to explain to me, as well as maybe give me a second example just to clarify even more with drawings (visuals) and explanations.arrow_forwardPart 1. Aqueous 0.010M AgNO 3 is slowly added to a 50-ml solution containing both carbonate [co32-] = 0.105 M and sulfate [soy] = 0.164 M anions. Given the ksp of Ag2CO3 and Ag₂ soy below. Answer the ff: Ag₂ CO3 = 2 Ag+ caq) + co} (aq) ksp = 8.10 × 10-12 Ag₂SO4 = 2Ag+(aq) + soy² (aq) ksp = 1.20 × 10-5 a) which salt will precipitate first? (b) What % of the first anion precipitated will remain in the solution. by the time the second anion starts to precipitate? (c) What is the effect of low pH (more acidic) condition on the separate of the carbonate and sulfate anions via silver precipitation? What is the effect of high pH (more basic)? Provide appropriate explanation per answerarrow_forwardPart 4. Butanoic acid (ka= 1.52× 10-5) has a partition coefficient of 3.0 (favors benzene) when distributed bet. water and benzene. What is the formal concentration of butanoic acid in each phase when 0.10M aqueous butanoic acid is extracted w❘ 25 mL of benzene 100 mL of a) at pit 5.00 b) at pH 9.00arrow_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





