8.E, Write the main products of the synthesis reaction according to the specified raw materials, reagents and reaction condition SnCl4 0°C Br 7. ÓMe Lon EtgN/CH2Cl2 он HaN
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A: HYDROLYSIS OF ALKENE IS NOT OXIDATION REACTION.
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A:
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Q: 159. What is the correct structure of product of the substitution reaction below: Hy HcC Br S Na +
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- A hydrocarbon of unknown structure has the formula C8H10. On catalytic hydrogenation over the Lindlar catalyst, 1 equivalent of Η2 is absorbed. On hydrogenation overa palladium catalyst, 3 equivalents of Η2 are absorbed. (a) How many degrees of unsaturation are present in the unknown structure? (b) How many triple bonds are Present? (c) How many double bonds are present? (d) How many rings are present? (e) Draw a structure that fits the data.There are two isomeric cyclohexa-1,4-diene products when benzoic acid undergoes the Birch reduction (see Problem 25.24). (a) Draw the mechanism that leads tothe formation of the major product. (b) Will the Birchreduction of benzoic acid occur faster or slower than theBirch reduction of benzene itself? Hint: Is –CO2H anelectron-donating or an electron-withdrawing group?Please help with the following ochem mechanisms.... 1. Provide the stepwise mechanisms for the following reactions (see attached picture)
- the 1-pentyne is reacting with CH3CH2CH2Li, then with the ketone, and lastly with NH4Cl and H2O. someone pls explain this with the mechanism. thank you!Draw themajor product of this reaction. Ignore inorganic byproducts. PPC, CH2Cl2Are there any other possible products for the following reaction in catalytic H2SO4 and H2O?
- Plz do Asap...! make reaction in 3 stepsWhat happens when anisole reacts with HNO3 and H2SO4? What about when those are followed by Br2 and FeBr3? Looking at the images, what are the major products?Chemistry Complete the following synthesis reactions. Fill in starting materials, reagents and/or products as needed. Show appropriate stereochemistry
- One possible way of determining the identity of an alkene, is to let itundergo an oxidative cleavage reaction in the presence of hot basicpotassium permanganate. You are given two containers said to containdifferent alkenes. Container A is marked as cis / trans‐2‐butene andcontainer B as 2‐methyl‐1‐butene. Explain by referring to the formation ofproducts, how you would verify the identity of the alkenes.1. what is the Nature of the leaving group (LG)? 2. what is the relative size of activation energy (Ea) for each reaction? 3. what is the Hammond's postulate? 4. what are the Relative thermodynamic stability of the reactive intermediates? 5. what is Influence of the solvent (if given) on the reactions and intermediates?My apologies. There was an error for the names. Reaction 1 and 2 are different. Possible answers for Reaction 1 are (choose 1): A. Acidification, B. Oxidation, C. Reduction, D. None of the choices Possible answers for Reaction 2 are (choose 1): Choices: A. FC Acylation, B. SN Alkylation, C. FC Alkylation, D. None of the choices