(a)
Interpretation: The IUPAC name of the following compound should be determined:
Concept Introduction:
In order to give the IUPAC name to the
1. The parent (longest) continuous carbon chain is identified.
2. The ending of the parent chain for alkane (-e) is -ane.
3. Name should be written in alphabetical order and numbering should be done in such a way that the substituent group gets lowest number.
4. Hyphen is used to connect the number to the name.
For number of carbons atoms in alkane chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec
(b)
Interpretation: The IUPAC name of the following compound should be determined:
Concept Introduction:
In order to give the IUPAC name to the alkane following steps are followed:
1. The parent (longest) continuous carbon chain is identified.
2. The ending of the parent chain for alkane (-e) is -ane.
3. Name should be written in alphabetical order and numbering should be done in such a way that the substituent group gets lowest number.
4. Hyphen is used to connect the number to the name.
For number of carbons atoms in alkane chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec
(c)
Interpretation: The IUPAC name of the following compound should be determined:
Concept Introduction:
In order to give the IUPAC name to the alkane following steps are followed:
1. The parent (longest) continuous carbon chain is identified.
2. The ending of the parent chain for alkane (-e) is -ane.
3. Name should be written in alphabetical order and numbering should be done in such a way that the substituent group gets lowest number.
4. Hyphen is used to connect the number to the name.
For number of carbons atoms in alkane chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec
Want to see the full answer?
Check out a sample textbook solution
Chapter 17 Solutions
EBK BASIC CHEMISTRY
- What is the missing intermediate 1 and the final product 2. Please include a detailed explanation explaining the steps of malonic ester synthesis. Please include drawings of the intermediate and how it occurs and how the final product is former.arrow_forwardWhat would be the reagents and conditions above and below the arrow that will complete the proposed acetoacetic ester synthesis? If it cannot be done efficiently, then I will choose that answer. There could be 2 or 4 reagents involved. Please provide a detailed explanation and drawings showing how it would proceed with the correct reagents.arrow_forwardFor benzene, the ∆H° of vaporization is 30.72 kJ/mol and the ∆S° of vaporization is 86.97 J/mol･K. At 1.00 atm and 228.0 K, what is the ∆G° of vaporization for benzene, in kJ/mol?arrow_forward
- The reaction Q(g) + R(g) → Z(l) is shown to be exothermic. Which of the following is true concerning the reaction. it is spontaneous only at High T, it is spontaneous at low T it is nonspontaneous at all T it is spontanrous at all T. it is non spontaneous only at low T.arrow_forwardThe reaction Q(g) + R(g) → Z(l) is shown to be exothermic. Which of the following is true concerning the reactionarrow_forwardWhich of the following has the largest standard molar entropy, S° (298.15 K) He H2 NaCl KBr Hgarrow_forward
- Which of the following is true for a particular reaction if ∆G° is -40.0 kJ/mol at 290 K and –20.0 kJ/mol at 390 K?arrow_forwardWhat is the major product of the following reaction? O O OH OH 1. BH 2. H₂O₂, NaOH OH OHarrow_forwardDraw the products formed when each ester is hydrolyzed with water and sulfuric acid.arrow_forward
Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning
Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning
Introductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning