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- What steps are needed to prepare phenylacetylene, C6H5C = CH, from each compound: (a) C6H5CH2CHBr2; (b) C6H5CHBrCH3; (c) C6H5CH2CH2OH?I recovered 3 mL of water, how many grams of water was produced in the reaction please show how? Cyclohexanol can attack the carbocation intermediate formed during the synthesis of cyclohexene. Draw this side product with the molecular formula C12H22O.(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 these
- Indicate the product of each reaction belowGive the following reaction A+3B --->2C.2) What is the main product for each of the following reactions? (d) Styrene + CH3CH2COCl AlCl3, then Br2, Fe -----> ? (e) Benzene + 1-chloro-2,2-dimethylpropane, AlCl3 -----> ? (h) Benzene + HCOCl, AlCl3 then 1-chlorobutane, AlCl3 -----> ?
- Give the major organic product(s) for each step in the following reactions (g,h,i,j)M 6 write the principal product in a, c & e and the neccesary reactives for b, d & f in the following reactions :Which of the following is the product of the reaction shown in Image 17? a. (C6H5)3COH b.C6H5CH2OH c.(C6H5)3CH d.(C6H5)2CHOH