why is the answer C? Wouldn't 5 be meso? please explain each answer if you can...
7. (9 pts) (Are the following optically active or meso? meso HyCHC OH HO opticaly actve active opti call active 8. (3 pts) How many stereoisomers are there of 2,3-dibromobutane? 4 sleeoisamvers (8 pts) Circle the letter of the statements that are true. a. Racemic mixtures are optically active Enantiomers have specific rotations that are equal, but have opposite signs 9. o adtc) Achiral molecules are optically inactive d Meso compounds contain equal amounts of enantiomers 4pts) Complete the Fischer...
Please answer all three if possible but mainly number 5 Br SCHLECH, 3. Assign R or Sconfiguration to the following molecules: Br F H. I H Br CH F F I . CH2CH3 CH2CH3 CH3CH -CH3 OH CH=CH2 H3C Сн, H "CH(CH3)2 4. Label each pair of stereoisomers below as A,B,C,D a Enantiomers b. Diastereomers c. identical d. Meso Compounds GH 5. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate...
need help on the last hw problems please explain and answer 43. An unknown compound of formula CeH16 was found to be optically active. On catalytic reduction of the unknown compound over a palladium catalyst, 2 equivalents of hydrogen were absorbed. Ozonolysis of the unknown compound gave two products: one was identified as an optically active dialdehyde of formula CsHaO2; the other compound was identified as acetaldehyde (CH3CHO). The most likely structure of the unknown compound is B. CH.CH-CH-CHECH CH...
My teacher is that A is not the major product. please explain why and what would be the major 22) (9 points) For the following reaction: a. (5 points) Draw a complete and detailed mechanism for the process shown below to form compounds A and B. mention whether it is initiation, propagation or termination. b/ (2 points) Explain why this reaction gives a mixture of compounds A and B and does not give compound C c. (2 points) Which product...
Can you guys tell me the exact answer and why that is the answer? Please and thank you! Question 2: Circle all that apply for a 50:50 mixture of these compounds. Optically active Not optically active Mixture of diastereomers same molecule does not Racemic mixture Both chiral pertgin to this Both achiral
Can you explain why the answer is enantiomers... For the following pair of compounds, indicate whether they are enantiomers, diastereomers, constitutional isomers or identical. Br City CH3 CH2CH3 H3C— Br and and H H3cqcH2CH3 Cl CH3
4. Multiple Choice Place your answer in the space provided. (2 pts. each; 12 pts. total) Which is NOT true of the aldol condensation? A. It accomplishes the formation of a new carbon-carbon bond B. The enolate is favored at equilibrium (assume NaOH as the base) C. The key step is the mechanism is attack of the enolate ion on a carbonyl carbon atom D. Dehydration of the aldol product is often observed and is irreversible. _Which sets of hydrogen...
I only need help with 5D) , please explain the thinking behind the rationale 5. Consider the reaction shown below: H CH3 Brg/ CH2Cl2 C=C meso-2,3-dibromobutane (as the sole product) Hac H a) Provide below a step-by-step mechanism for that reaction (10 points) When the reaction above is carried out with 1-phenyl-1-propene, four products are formed: | H Ph C=Ć Brz/ CH2Cl2 Br. Br BECOMH (19%) HU HECH Br Ph ul.C-CAH 181%] and нус Br (+ enantiomer) Hac Pn (+...
please help solve question 10 and question 11. thank you [2] QUESTION 10 Which of the following statements is correct? A B (1) and (2) are optically active, (3) and (4) are meso thus optically inactive 1) and (2) are optically active, (3) and (4) are meso thus optically active too (1) and (2) are meso thus optically inactive, (3) and (4) are optically active All the compounds are optically active. с D [2] QUESTION 11 Which of the following...
Please explain why or why not A B C and D can be displaced! thanks! 4. X is a potential leaving group and could be displaced by the following reaction. + X Indicate if X is displaced when a. CH CH3 161.. b. Br c. OH and d. OCOCH3