Q7. What product is formed when the following compound is subjected to heating? A) B) C) Both products are formed. Give detailed Solution with explanation needed with structure, don't give Handwritten answer D) None of the given product is formed
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- Identify the pericyclic reactions in the followingreaction schemes. Give the complete reaction name and indicate the course of the reaction with the aid of the arrow notation.provide the major profucts ( wrote "no reaxtion "if you think so) for the following reactions with correct stereochemistry. Please explain step by step with explanationIdentify the pericyclic reactions in the followingreaction schemes. Give the complete reactionname and indicate the course of the reaction withthe aid of the arrow notation.
- Give a clear handwritten answer with explanation..give the mechanism of given bleow below reaction with perfect reagents ?Provide the curved arrow fomalism for the compound shown below treated with Br2 in water and include transition states. Thank you for the help! I really apprecitate it.Need solution to all parts urgently I'll surely upvote for correct ans otherwise dislike provide an acceptable IUPAC and indicate any stereochemistry where appropriate...
- The spirocyclic pentadiene derivative F shown below is converted stereospecificallyinto compound G on heating. The transformation involves two consecutive pericyclicreactions of the same type, and proceeds via compound H which is not isolated. Identify the type of pericyclic reaction occurring, and determine the structure ofcompound H.arrange the following molecules in an order from least to greatest reactivityArrange the following compounds in increasing reactivity towards E+.
- cis-4-Bromocyclohexanol and trans-4-bromocyclohexanol form the same elimination product but a different substitution product when they reactwith HO-. a. Why do they form the same elimination product?b. Explain, by showing the mechanisms, why different substitution products are obtained.c. How many stereoisomers does each of the elimination and substitution reactions form?Show the curved-arrow mechanism for the first step, and the structure of the cyclic intermediate formed, when cyclopentene in treated with KMnO4 . A Lewis structure for the permanganate ion is provided in the hint. Make sure to show all non‑bonding electron pairs and formal charges where necessary. Omit K+ .Provide the curved arrow mechanism for the reaction of the compound shown below treated with Cl2/FeCl3. Include transition states and the major product. I apprecitate the help