Answer to question 8) the synthesis of p-nitrotoluene from
benzene is shown below.
8. Design a synthesis of p-nitrotoluene, starting from benzene (3 pts). from to NO2 4 9....
Are the following pairs identical, enantiomers, diastereomers, or constitutional isomers? Sort these pairs into the proper categories. Are the following pairs identical, enantiomers, diastereomers, or constitutional isomers? Sort these pairs into the proper categories. Reset Help HC=CH2 CH2CH3 CH3 and CH3CH2H U CH,OH CHCH H-CH3 and CHH CH2CH3 CH OH CH3 HOCHZ H HC=CH2 CH3 CH3 CH,CH, CH3 CH,CH3 Ho-H ood HO-FH || - ci and H- C1 CH2CH3 HOH and H-OH H- Cland CiH CH3 CH and CH3 and...
Stereochemistry Questions Name: CHE 201 Date: 1. Describe the relationship between the pairs of compounds as: E- Enantiomers D-Diastereomers [-Identical Structures C-Constitutional Isomers Hs CH.CH -н HO- H но # and - H- H- ci CH,CHE Br -*-* and CH Br H / OH and CH3 HO BrH2C H3C CHE CH2CH3 CICH CH3 H3CKH HOCI CH2CH3 CH3
Question 9 15 pts Determine the relationship between each set of structures Set 1: identical Set 2: constitutional isomers Set 3: diastereomers Set 4: diastereomers Set 5: enantiomers 2 OH OH OH e HO... г - 2 ОН ОН ОН Но... 3 ОН Н. СІ НО, CI нс H нс ОН ОН H 5 н- H CHO -ОН ОН CH2OH CHO но- -Н Н- -ОН Сн,ОН Е.
5. (3 pts each) For the following pairs of molecules, indicate if they are identical different compounds. enantiomers, diastereomers, or constitutional isomers CHE CH H3COH and HOT но — сня нас — Br Hc- Br CH2OH Леон нон он and a нус он Он но- нс сня CI HOBO но and нстве
Chem 255 - Chapter 5 Worksheet.pdf of the pairs of molecules as either identical, constitutional isomers, enantiomers, diastereo or not identical isomers? Explain your answer. Он OH z z mega Dashboard 6 Calendar E TODO Nostratie 1 CI нс н C=C HyCCH(CH3)2 Hн CEC н "Br H C C(CH3)3 CH3 Hic Hoc НАС CH CH OH Н -ОН H-1 -он снон CH2OH но -н НО- н Сн,он CHO HI-он H-I-OH сон CHO но -н HO-IH Сньон
3. Identify the relationship between each of the following pairs of molecules as constitutional isomers, enantiomers, diastereomers, or meso compounds. CH3 но - оноо но Х он но -н. H2NH H- H CH3 осон BiH HO н+он н-он ну он Br +н CH3 CH3 HOTH HO HỌ NH2 NH, HẠNH I но НЕН CH3 I H- H нон н +он но -н CH3 HO на
What is the proper systematic name for the following compound, including the appropriate stereochemical designation? Please answer carefully, credit will only be given if name is exactly correct. ie: no spelling mistakes; hyphens and commas in the right places etc... Tries 0/1 Submit Answer What is the proper systematic name for the following compound, including the appropriate stereochemical designation? OH Please answer carefully, credit will only be given if name is exactly correct. ie: no spelling mistakes; hyphens and commas...
Design a synthesis of n-propylbenzene from benzene. Hint: A one-step synthesis using CH,CH CH Br and AlBr yields a large amount of isopropylbenzene. 4. 5. Design a high-yield synthesis of each target starting from benzene NO2 NH2 NH2 H2N CI CI target target target target
Starting from benzene and using any other necessary reagents of your choice, design a synthesis for each of the following compounds. Some problems have more than one plausible 1. answer (g)* in this example, what can be done to minimise the amount of the meta/para isomes. NO2 (h) रेर Br (i) Н-N. Br NH2 (k) Br "SoH
7.Shown below are structural diagrams for five pairs of molecules. From the list of five terms (enantiomers, diastereomers, conformers, constitutional isomers, identical), choose the single term that best describes each pair. Note that a term may be used more than once if necessary. CH2CH3 CH3 i) Br CH3 and F-CH2CH3 Br ti CH3 《XY CH3 IX tx tx Br DX BrOH CH3 CH3 iv) and HOH Cl Br Br CH3 CH3 and H_Br CH3 -H v) Br CH3 IX CH3