In each reaction box, place the best reagent and conditions from the list below. There is more than one possible route. Note: İf one or more reagents are incorrectly placed, a single red X will appear on the top left. 1) Н, 2) 3) 4) 5) Br но 6) 1. CH3(CH2)2MgBr, 2. H2O 1. CH3CH2CH2CHO, 2. H2O PCC CH3(CH2)2OH 1. CH3MGB., 2. H2O CH3B Нзо* НОСH-CH2ОH, н* 1. CH3CHO, 2. Но Mg

In each reaction box, place the best reagent and conditions from the list below. There is more than one possible route. Note: İf one or more reagents are incorrectly placed, a single red X will appear on the top left. 1) Н, 2) 3) 4) 5) Br но 6) 1. CH3(CH2)2MgBr, 2. H2O 1. CH3CH2CH2CHO, 2. H2O PCC CH3(CH2)2OH 1. CH3MGB., 2. H2O CH3B Нзо* НОСH-CH2ОH, н* 1. CH3CHO, 2. Но Mg

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...

See similar textbooks

Similar questions

Complete the following reaction O NH₂ CH3 NH₂ CH3 Br CH3 NH₂ CH3 NH 2 CH₂ Br 1) HNO/H₂SO4 2) HBr/CuBr NO₂ Br NO₂
2. For each synthetic step, provide the reagents needed to perform the transformation. A NH2 ii O iii
Select the arrow drawing that best describes this step of an E1 reaction. H I-0: н. Oi O ii O iii O iv нн H3C I i CH3 нн H3C CH3 I-0: н. I H3C I H нн нн H3C CH3 iv CH3
1. Propose multi-step syntheses to make the products shown below. Separate the steps with numbers. You should think about the product after each step you propose to make sure the scheme will work. Use the summary of reactions at the end of Ch 8,9, 10, 11, 17 to help you. Count the number of carbons in the reagents and products. A) OH .CI B) ??? HO. C) H2 .C ??? CH3 CH3CCCH3 H3C `CH3 Но
7. Predict the product and draw the 2-step mechanism. 1. ROH attacks ZnCl2, giving the O-atom a (+) charge and Zn a (-). The ZnCl, does not lose a CI- ion, it's simply attached to the OH group. 2. Then a CH ion attacks and kicks off the better leaving group (Sn2). ZnCl2 HO
Explain well with proper step by step Answer.
4. Fill in the boxes with the reactants, reagents, or products for each reaction. Underneath each reaction, propose a complete mechanism for the transformation. Ph NH₂ B & B & (there is excess of all reagents) 1. CH₂l (excess) 2. Ag₂O 3. heat Br₂ NaOH 1. NaNHz 2. H3O+
What is the best reagent for carrying out the reaction shown below?
Show the product formed in each step of this multi-step synthesis.
9. Mechanism: Propose a mechanism for the following transformation. Br Br H2O
3. Draw all products for the following reactions. For your products, write whether the nucleophile added to the Re face or Si face of the starting material. a. HO b. 1) LIAIH 2) H™ 1) CH3CH2Li 2) H+ c) Determine whether the nucleophile added to the Re face or Si face of benzaldehyde.
Give the major product of the following reaction. Br, (1 equiv.) ? hv -Br Br Br- Br There is no reaction under these conditions or the product is not listed here. Br Br Br Br Br