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A: To Find :- The major product of the given reaction.
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Q: Question attached
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Q: Identify the major product for the following reaction
A: given identify major products
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- 27. Which of the following reactions gives the product shown? Select all that apply.QUESTION 4Predict the products(s) from the reaction of 1-hexyne with each of the following reagents:a) 1 mole of HBrb) H2O, H2SO4, HgSO4c) 2 moles of Br2d) Excess Cl2e) 2 moles of HCl with H2O2f) 1 mole of HClDraw the product(s) of the reaction between 1-propyne (1 mole) and the reagents given below. C) excess H2 in Lindlar’s catalyst D) NaNH2 E) H3O+
- (CH3)3CHOH is reacted with CH3-O-C--C6H5 in a transesterification reaction. What is the M+ of the product? || O 102 80 178 None of theseHURRY ASAP I WILL RATE NO NEED FOR EXPLANATION WHICH OPTIN Which one of the following alcohols can not be oxidized in use of KMnO4 solution as oxidizing agent? RCH(CH3)OH RCH2CH(OH)CH3 RCH(OH)R R3COH RCH2OHWhen (CH3CH2)3CBr is added to CH3OH at room temperature, the product is(CH3O)C(CH2CH3)3. Propose a mechanism(s) for the reactions leading to theseproducts and use curved arrows to show the movement of electrons.
- What i sthe major product of the reduction of the following compund with LiAlH4? The correct answer is C, but please explain why.Chemistry 60. Give the principal product(s) expected, if any, when trans-1,3-pentadiene reacts under the following conditions. Assume one equivalent of each reagent reacts unless noted otherwise. (a) H2O, H3O+ (b) Na+EtO- in EtOH (c) Maleic anhydride heatA 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.
- 12. Draw the structure of the major organic products for each reaction below. Indicate the stereochemistry. If there is no reaction write down “no reaction” please ASAP its due soon. thanks![VI2&3] Instructions: Provide the missing reagent/s, substrate/s, or product/s for each reaction. (refer to the photo below)3. Prepare each compound from cyclopentanol. More than one step may be needed.llustrate the mechanism of the reaction. Include the intermediate product and by-product formed in the reaction. (see attached photo)