Н. H H H2 Н H₂ CH3 Н CH3 'H

Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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What is the iupac name of this Newman projection 

The image shows a chemical structure diagram of trans-decalin in its chair conformation. The diagram consists of two cyclohexane rings connected at two adjacent carbon atoms. 

- Each cyclohexane ring is in a chair conformation, which is a common three-dimensional structure that provides stability.
- The hydrogen atoms (H) are shown attached to the carbon atoms of the rings. 
- Notably, a methyl group (CH₃) is attached to one carbon on each ring.
- The trans conformation is characterized by the methyl groups on opposite sides along the hydrogenation axis of the interconnected rings.

This arrangement of trans-decalin typically results in a more stable molecule compared to the cis conformation due to reduced steric hindrance. The depiction highlights the spatial arrangement and is critical for understanding stereochemistry in organic chemistry.
Transcribed Image Text:The image shows a chemical structure diagram of trans-decalin in its chair conformation. The diagram consists of two cyclohexane rings connected at two adjacent carbon atoms. - Each cyclohexane ring is in a chair conformation, which is a common three-dimensional structure that provides stability. - The hydrogen atoms (H) are shown attached to the carbon atoms of the rings. - Notably, a methyl group (CH₃) is attached to one carbon on each ring. - The trans conformation is characterized by the methyl groups on opposite sides along the hydrogenation axis of the interconnected rings. This arrangement of trans-decalin typically results in a more stable molecule compared to the cis conformation due to reduced steric hindrance. The depiction highlights the spatial arrangement and is critical for understanding stereochemistry in organic chemistry.
Expert Solution
Step 1

For IUPAC naming following steps are required -

  • First of all identify the longest carbon chain containing functional group.
  • Start numbering from the side from  which functional group or substituents got least number.

 

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