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Concept explainers
(a)
Interpretation: The name of the given compound has to be determined.
Concept introduction:
Naming of Cycloalkane using
Use the Cycloalkane name as the parent.
Cycloalkanes are named as alkyl-substituted cycloalkanes rather than as cycloalkyl-substituted
Identify and number the substituents.
The group which has alphabetical priority should be numbered first and proceed around the ring in a direction in which the second substituent gets the lowest possible number.
The order of priority is,
The IUPAC name for the ketone is written by replcing the ‘e’ of alkane to ‘one’
Compound which has two ketone groups are diones
(b)
Interpretation: The name of the given compound has to be determined.
Concept introduction:
Naming of Cycloalkane using IUPAC nomenclature:
Use the Cycloalkane name as the parent.
Cycloalkanes are named as alkyl-substituted cycloalkanes rather than as cycloalkyl-substituted alkanes. There is no need to assign a number if there is one substituent on the ring.
Identify and number the substituents.
The group which has alphabetical priority should be numbered first and proceed around the ring in a direction in which the second substituent gets the lowest possible number.
The order of priority is,
Ketone: Ketone is a group of organic compound where two aryl or alkyl groups are connected by a carbonyl group. It is represented as
The IUPAC name for the ketone is written by replcing the ‘e’ of alkane to ‘one’
Compound which has two ketone groups are diones
(c)
Interpretation: The name of the given compound has to be determined.
Concept introduction:
IUPAC naming for Alkane:
- Name the main chain: Find the longest carbon chain and name the chain according to the number of carbon atoms it contains; is also the suffix part of the name.
- Number the carbon atoms in the main chain: The carbons are numbered, in which the substituents must get lowest possible numbers.
- Identify the substituents, and number each: The number at where substituents are present has to be noted. The substituents written as prefix.
- Write the names as a single word: Use the hyphen to separate the numbers from the different prefix; commas to separate numbers. If two or more different substituents are present, arrange them in alphabetical order. If two or more identical substituents are present, use prefixes di-, tri-, tetra-, but this particular prefix should not be used for alphabetizing purpose.
According to IUPAC nomenclature, the naming of compound is determined by the priority of the
The order of priority is,
Ketone: Ketone is a group of organic compound where two aryl or alkyl groups are connected by a carbonyl group. It is represented as
The IUPAC name for the ketone is written by replcing the ‘e’ of alkane to ‘one’
Compound which has three ketone groups are triones
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Chapter 19 Solutions
Organic Chemistry
- टे Predict the major products of this organic reaction. Be sure to use wedge and dash bonds when necessary, for example to distinguish between different major products. ☐ ☐ : ☐ + NaOH HO 2 Click and drag to start drawing a structure.arrow_forwardShown below are five NMR spectra for five different C6H10O2 compounds. For each spectrum, draw the structure of the compound, and assign the spectrum by labeling H's in your structure (or in a second drawing of the structure) with the chemical shifts of the corresponding signals (which can be estimated to nearest 0.1 ppm). IR information is also provided. As a reminder, a peak near 1700 cm-1 is consistent with the presence of a carbonyl (C=O), and a peak near 3300 cm-1 is consistent with the presence of an O–H. Extra information: For C6H10O2 , there must be either 2 double bonds, or 1 triple bond, or two rings to account for the unsaturation. There is no two rings for this problem. A strong band was observed in the IR at 1717 cm-1arrow_forwardPredict the major products of the organic reaction below. : ☐ + Х ك OH 1. NaH 2. CH₂Br Click and drag to start drawing a structure.arrow_forward
- NG NC 15Show all the steps you would use to synthesize the following products shown below using benzene and any organic reagent 4 carbons or less as your starting material in addition to any inorganic reagents that you have learned. NO 2 NC SO3H NO2 OHarrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forwardShow work...don't give Ai generated solutionarrow_forward
- 1 Please provide an efficient synthesis of the product below from the starting material. Use the starting material as the ONLY source of carbon atoms. Show the synthesis of each compound that would be used in the overall synthesis of the product. [This synthesis uses alkyne and alcohol chemistry.]arrow_forward10- 4000 20 20 30- %Reflectance 60 50- 09 60- 40- Date: Thu Feb 06 17:30:02 2025 (GMT-05:0(UnknownP Scans: 8 Resolution: 2.000 70 70 88 80 3500 3000 2500 90 100 00 Wavenumbers (cm-1) 2000 1500 2983.10 2359.13 1602.52 1584.22 1451.19 1391.87 1367.07 1314.37 1174.34 1070.13 1027.33 1714.16 1269.47 1000 1106.08 1001.14 937.02 873.60 850.20 780.22 686.91 674.38 643.09 617.98 02/06/25 16:38:20arrow_forwardd. Draw arrow-pushing mechanism for an enzymatic retro-aldol reaction of the following hexose. Use B: and/or HA as needed. OH OH سية HO OH OHarrow_forward
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