
(a)
Interpretation:
The structure of
Concept introduction:
The systematic naming of organic compound is given by
Rules for writing IUPAC name from the structural formula are given below.
- First, identify the longest carbon chain.
- The next step is to identify the groups attached to the longest chain.
- Identify the position, location, and a number of the substituents bonded to the carbon chain.
- Use prefix di, tri, tetra if the same type of substituents is present.
- Name the substituents in alphabetical order.
- In the heterocyclic compound, azo for nitrogen, oxo for oxygen, thio for sulfur and so on is used.

Answer to Problem 26.1P
The structure of the given compound,
Explanation of Solution
The name of the given compound
Figure 1
The structure of the given compound,
(b)
Interpretation:
The structure of
Concept introduction:
The systematic naming of organic compound is given by IUPAC nomenclature. The naming of organic compound is done such that the structure of the organic compound is correctly interpreted from the name.
Rules for writing IUPAC name from the structural formula are given below.
- First, identify the longest carbon chain.
- The next step is to identify the groups attached to the longest chain.
- Identify the position, location, and a number of the substituents bonded to the carbon chain.
- Use prefix di, tri, tetra if the same type of substituents is present.
- Name the substituents in alphabetical order.
- In the heterocyclic compound, azo for nitrogen, oxo for oxygen, thio for sulfur and so on is used.

Answer to Problem 26.1P
The structure of the given compound,
Explanation of Solution
The given compound
Figure 2
The structure of the given compound,
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Chapter 26 Solutions
Organic Chemistry
- 1. For each of the reaction "railroads" below, you are either asked to give the structure(s) of the starting material(s) or product(s), or provide reagents/conditions to accomplish the transformation, as indicated by the boxes. a. NaOMe H+ .CO,H HO₂C MeOH (excess) MeOH H3C Br يع CH3 1. LiAlH4 2. H3O+ 3. PBг3 H3C 1. Et-Li 2. H3O+ -CO₂Me -CO₂Me OH CH3 CH3 ল CH3arrow_forwardPredict the intermediate 1 and final product 2 of this organic reaction: NaOMe ག1, ད།་, - + H You can draw 1 and 2 in any arrangement you like. 2 work up Note: if either 1 or 2 consists of a pair of enantiomers, just draw one structure using line bonds instead of 3D (dash and wedge) bonds at the chiral center. Explanation Check Click and drag to start drawing a structure. Х © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Parrow_forwardWhat is the total energy cost associated with the compound below adopting the shown conformation? CH3 HH DH CH3arrow_forward
- ΗΝ, Draw Final Product C cyclohexanone pH 4-5 Edit Enamine H3O+ CH3CH2Br THF, reflux H Edit Iminium Ionarrow_forwardHow many hydrogen atoms are connected to the indicated carbon atom?arrow_forwardIdentify the compound with the longest carbon - nitrogen bond. O CH3CH2CH=NH O CH3CH2NH2 CH3CH2C=N CH3CH=NCH 3 The length of all the carbon-nitrogen bonds are the samearrow_forward
- Identify any polar covalent bonds in epichlorohydrin with S+ and 8- symbols in the appropriate locations. Choose the correct answer below. Η H's+ 6Η Η Η Η Η Ηδ Η Ο Ο HH +Η Η +Η Η Η -8+ CIarrow_forwardH H:O::::H H H HH H::O:D:D:H HH HH H:O:D:D:H .. HH H:O:D:D:H H H Select the correct Lewis dot structure for the following compound: CH3CH2OHarrow_forwardRank the following compounds in order of decreasing boiling point. ннннн -С-С-Н . н-с- ННННН H ΗΤΗ НННН TTTĪ н-с-с-с-с-о-н НННН НН C' Н н-с-с-с-с-н НН || Ш НННН H-C-C-C-C-N-H ННННН IVarrow_forward
- Rank the following compounds in order of decreasing dipole moment. |>||>||| ||>|||>| |>|||>|| |||>||>| O ||>>||| H F H F H c=c || H c=c F F IIIarrow_forwardchoose the description that best describes the geometry for the following charged species ch3-arrow_forwardWhy isn't the ketone in this compound converted to an acetal or hemiacetal by the alcohol and acid?arrow_forward
- Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
