The answer:
The explanation of the an bove answer lies in the following image, please have a look.
Thank you in advance. Much appreciated. Consider the dehydration of the following alcohols using a strong...
please explain in detail. Thank you in advance .
1. Circle the mechanism (SN2, SN1, E2, or E1) responsible for the formation of each product in this reaction. If the product cannot be formed in the reaction, circle "not a product". (2 pts) CI CHE CH3 CHE CH3 осна SN2 SN1 E2 E1 S2 SN1 E2 E1 SN2 Sn1 E2 E1 SN2 SN1 E2 E1 not a product not a product not a product not a product 2. These reactions...
Showing mechanism and major product is extremely appreciated.
Thank you in advance!
B) Predict the products for the reactions below (2 points per box, 4 points total section). MgBr SH Major product Major product C) Solve the following boxes below (2 points per box, 6 points total section). 1 equiv HNMez HH 0 LDA
show all work please thank you!!!
3. (10 pts total) Consider the following alkene addition reaction: Brz H2O НО Br a. (3 pts) This type of alkene addition reaction is mediated by both Lewis acids and bases. Of the two inorganic reactants (Br2 and H2O), place a triangle (1) around the one which functions as a Lewis acid in the above transformation b. (3 pts) of the two regioisomeric reaction products shown, only one is observed to form under the...
Both problems please, thank you very much in
advance!
3. Propose arrow.pushing mechanisms to explain the formation of each product. TOCH Emper EtMgBr LOCH, OCH och H2O H30*
Experiments Dehydration of 2-methylcyclohexanol Questions 1. Please answer this question on notebook paper, not in the lab sometimes dimicult to read.) tebook (carbon copies are Consider the phosphoric acid-catalyzed dehydration of the following list of nine alcohols. Give the structure of each alcohol and that of the resultant alese. If a MIXTURE of alenes is anticipated. give both products and circle the major product (a) Cyclohexanol: (b) 1-methylcyclohexanol (c)2-methylcobecnold 3-methylcyclohexanol: (e) 4-methylcyclohexanol: (cyclopentanol (R) 3- canotth) 2-pentano: 0) 3-pentanol. 2....
Thank you so much!
(2 pts) Draw the major elimination products and Identify the mechanism responsible (E1 or E2). If both E and Z isomers form, only draw the E alkene. If only one isomer forms, label the alkene "E,""Z," or neither 1. NaOCH3 а. Br НОСHЗ b. НОСНЗ C. CI NaOCH3 d. (6 pts) Draw the substitution and/or elimination product(s) for the following reactions and identify 2. the mechanism responsible (SN1, SN2, E1, or E2) for each product drawn....
Please answer all. thanks
QUESTION 5 HO Reaction C Reaction D Consider the structural changes that take place during Reaction C and Reaction D and the fundamental mechanisms that you identified from the previous question. Fill in the boxes with the missing reagent that is required to complete Reaction C and Reaction D? (Choose only one reagent per reaction.) O Reaction C: HCI Reaction C: Cl2, heat Reaction C: SOCl2 with pyridine Reaction D: KOC(CH3)3 O Reaction D: NaOCH2CH3 Reaction...
Please answer ALL of them. Thank you so much in advance! 1. What is the probability of rolling snake eyes? 2. What is the probability of getting 2 boys and 2 girls in a family of 4 children (pascal's triangle is handy here) 3 Some says they have 2 children but they are not both girls, knowing that what are the odds that they are both boys? 4. What are the odds of flipping a coin 5 times and getting...
4. For the following pairs of reactions, clearly circle the reaction you believe would occur foster Briefly, using chemical principals, describe in the space below why you made your decision Also, indicate in the box which mechanism (S1, S2, E1, E2) would be the likely mechanism of the reaction you circled. (5 pts each) PHOSO CF, NaCN DMF Ph CN oso,CF, DMF Mechanism of circled reaction NaOme NaOme (E)-3-methyl-2-pentene - (Z)-3-methyl-2-pentene MeOH, A MeOH, A Mechanism of circled reaction KBr...
Please show the mechanism of the following reactions. Thank you so
much in advance!
Не осн, H5C, осна H5C Br + HBr CH3OH 25 °C 50% 50% H,0 . + Br° . . ~ + снҳон 60 °C + ~ ~ о но Br Acetone 50 °C . . .ю° сьон Д. но во 60 °C . в . сноснон , нве HBr 75 °C