**Title: Naming Organic Structures with Stereochemistry****Introduction:**For each of the following organic structures, determine a complete name using any acceptable method (common or IUPAC). Ensure that the name includes proper stereochemistry, where applicable.**Structures:**- **Structure (a):** - A chain of carbon atoms is shown with several substituents. The structure appears to be a substituted hydrocarbon with both alkyl and functional groups attached. Notably, it includes both a tertiary butyl group and an ethyl group among others.- **Structure (b):** - This structure includes a ketone functional group. There is a long carbon chain with various substituents, including a methyl group attached to one of the carbon atoms.- **Structure (c):** - The structure represents a cyclooctane ring with two substituents. One substituent is an alcohol (OH group) and the other is an isopropyl group attached with stereochemistry indicated by wedge and dash lines.- **Structure (d):** - A carbon chain with a bromine substituent and a ketone group is visible. The ketone is within a longer chain that includes multiple substituents and a secondary branching methyl group.- **Structure (e):** - This structure features a thiol (SH group) in addition to other substituents. Notable substituents include an ethyl group and a secondary butyl chain attached to a central carbon.**Instructions for Naming:**1. Identify the longest carbon chain in the structure to serve as the parent hydrocarbon.2. Identify and name all substituents attached to the main carbon chain.3. Use the appropriate suffixes for functional groups (e.g., -ol for alcohols, -one for ketones, -thiol for thiols).4. Assign correct numbers to the substituents following IUPAC convention to give the lowest possible numbers to the highest-priority groups.5. Indicate stereochemistry using prefixes like R/S or E/Z as appropriate when chiral centers or double bonds are present.6. Compile the name starting with the substituents in alphabetical order, followed by the base name of the compound with the suffix of the primary functional group.**Conclusion:**Accurate naming of these structures requires careful analysis of each compound's functional groups, stereochemistry, and substituents. Ensure consistency with IUPAC nomen

Given that : We have to give the IUPAC name of the following compounds :The IUPAC name of the above given compound is 2-(butan-2-yloxy)butane. The IUPAC name of the above given compound is 4-ethyl-3,5-dimethylhept-1-ene.The IUPAC name of the above given compound is (1R,4R)-4-tert-butylcyclooctan-1-ol.The IUPAC name of the above given compound is 3-bromo-6,6-dimethyloctan-4-one. The IUPAC name of the above given compound is 2-methoxy-4-methylhexane-2-thiol.

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For each of the following structures, give a complete name using any acceptable method (common or IUPAC). Be sure to include in your name proper stereochemistry, where appropriate. CH3CHCH CH;CH2CHOCHCH2CH3 a) b) CH3 CH3 CH;CH,CHCHCH2CH3 он CH3 CH3 c) d) CH3CH,CHCCH,CCH3 CH3 Br ČHĄCH3 CCH3 ČH3 CH2CH3 CH2CHCH3 CH3ČOCH3 SH

For each of the following structures, give a complete name using any acceptable method (common or IUPAC). Be sure to include in your name proper stereochemistry, where appropriate. CH3CHCH CH;CH2CHOCHCH2CH3 a) b) CH3 CH3 CH;CH,CHCHCH2CH3 он CH3 CH3 c) d) CH3CH,CHCCH,CCH3 CH3 Br ČHĄCH3 CCH3 ČH3 CH2CH3 CH2CHCH3 CH3ČOCH3 SH

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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