- #1
Hydrogentaion of Arene: Why Double Bond Not Broken?
- Thread starter somecelxis
- Start date
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Discussion Overview
The discussion revolves around the hydrogentation of a cyclic structure, specifically questioning why the double bond in the structure is not broken during the addition of hydrogen atoms. The focus appears to be on the structural and chemical properties of the compound in question.
Discussion Character
- Homework-related
- Debate/contested
Main Points Raised
- One participant questions why the double bond in the cyclic structure is not broken and why two hydrogen atoms are not added to it.
- Another participant challenges the identification of the structure as phenyl, asserting that it is not phenyl but cyclobutene.
- Further replies continue to dispute the identification of the structure, with one participant stating it is not cyclobutene either and requesting clarification on the correct structure.
- A later reply emphasizes the need to understand why the C=C double bond in the cyclic structure remains intact during the reaction.
Areas of Agreement / Disagreement
Participants do not appear to agree on the correct identification of the cyclic structure, with multiple competing views regarding its classification. The discussion remains unresolved regarding the reasons for the behavior of the double bond during hydrogentation.
Contextual Notes
There are limitations in the discussion related to the assumptions about the structure being discussed, as well as the lack of clarity on the specific chemical properties that influence the reaction.
![IMG_20140820_181752[1].jpg](/data/attachments/55/55580-3cd31bdc62b6b4deee17e5073f6762d2.jpg?hash=PNMb3GK2tN){kind=small}
![IMG_20140821_132527[1].jpg](/data/attachments/55/55600-a12bf4625fff799e4011a4c77cbf70cf.jpg?hash=oSv0Yl__eZ)
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