multiple steps H. https://ibb.co/HVSLHCZ e In the fourth step of the synthesis, the Grignard reagent (shown below) makes a new C-C bond with an appropriate molecule to make the alcohol product shown. Which of the following reaction partners would achieve this reaction? OH step 4: ? „MgX Et20 https://ibb.co/3vRxY1re https://ibb.co/2sSFVGMe https://ibb.co/tUZwTd4 e OH https://ibb.co/1LRSZP5 e https://ibb.co/Qn0xjdX https://ibb.co/SmDF4pq e

multiple steps H. https://ibb.co/HVSLHCZ e In the fourth step of the synthesis, the Grignard reagent (shown below) makes a new C-C bond with an appropriate molecule to make the alcohol product shown. Which of the following reaction partners would achieve this reaction? OH step 4: ? „MgX Et20 https://ibb.co/3vRxY1re https://ibb.co/2sSFVGMe https://ibb.co/tUZwTd4 e OH https://ibb.co/1LRSZP5 e https://ibb.co/Qn0xjdX https://ibb.co/SmDF4pq e

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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< Problem 49 of 52 Submit Draw the major product of this reaction. Ignore inorganic byproducts and the alcohol side product. سلا 1. excess PhMgBr 2. H2O Select to Draw Q
Three reactions between a Grignard reagent and a carbonyl compound are given. Draw the main organic product for each reaction and indicate if H+ or H¯ is needed to complete each reaction. The starting material structures are provided in the answer fields as a starting point for your drawings. The first reaction involves a ketone. 1. CH₂MgBr 2. H+ or H™? Select Draw / |||||| C Rings O More Erase
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Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound s synthesis requires only two steps enter "none" for step 3. OH `CH3 Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol Reagents available a. LIAIH4 f. PBr3 k. CH3 CH2 CH2 MgBr; then H3O+ b. Н>SO4 g. CrОз, Н, SO4, H,O 1. C6 H5 MgBr (phenylmagnesium bromide); then H3O+ с. НC h. NaH m. (CH3)2CHMgBr: then H30+ d. HBr i. CH3 MgBr; then H30+ n. Dess-Martin periodinane (DMP) e. SOCI2 j. CH3 CH2MgBr; then H3O+ Write the number/letters of the alchol/reagents in the boxes below.
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Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two steps enter "none" for step 3. OH Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol a. LiAlH4 f. PBr3 b. H₂SO4 c. HCI d. HBr e. SOC1₂ Reagents available g. CrO3, H₂SO4, H₂O h. NaH i. CH3 MgBr; then H3O+ j. CH3 CH₂ MgBr; then H3O+ k. CH3 CH₂ CH₂ MgBr; then H3O+ I. C6H5 MgBr (phenylmagnesium bromide); then H3O+ m. (CH3)2 CHMgBr: then H3O+ n. Dess-Martin periodinane (DMP) Write the number/letters of the alchol/reagents in the boxes below. Alcohol starting material 4 Reagent for step 1 n Reagent for step 2 j Reagent for step 3 c
Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two steps enter "none" for step 3. ů Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol a. LiAlH4 f. PBr3 b. H₂SO4 c. HCI d. HBr e. SOC12 g. CrO3, H₂SO4, H₂O h. NaH Reagents available i. CH3 MgBr; then H3O+ j. CH3 CH₂ MgBr; then H3O+ k. CH3 CH₂ CH₂ MgBr; then H30+ I. C6H5 Mg Br (phenylmagnesium bromide); then H3O+ m. (CH3)2 CHMgBr: then H3O+ n. Dess-Martin periodinane (DMP) Write the number/letters of the alchol/reagents in the boxes below. Alcohol starting material | Reagent for step 1 Reagent for step 2 Reagent for step 3
Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two steps enter "none" for step 3. OH Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4. 2-propanol 5. cyclohexanol a. LiAlH4 f. PBr3 g. CrO3, H2SO4, H₂O b. H2SO4 c. HCI h. NaH d. HBr i. CH3 MgBr; then H3O+ e. SOCl2 Reagents available j. CH3CH2MgBr; then H3O+ k. CH3CH2CH2 MgBr; then H3O+ I. C6H5 MgBr (phenylmagnesium bromide); then H3O+ m. (CH3)2 CHMgBr: then H3O+ n. Dess-Martin periodinane (DMP)
What is the major organic product formed in the following sequence of reactions? A, B, C, or D?