31 Multiple Choice Problems: 16 questions, 4 pts each =64 total. 1. Circle optically active molecules...
please answer all Question 1 2 pts Determine whether the molecule below is optically active. cannot determine O optically active O optically inactive Question 2 2 pts Determine the relationship between the two molecules below NH2 HO H3COOH identical enantiomers constitutional isomers diastereomers Question 3 2 pts Determine the relationship between the two molecules below H HOW enantiomers O identical constitutional isomers diastereomers D Question 4 2 pts Determine the total number of stereoisomers represented by the bond line drawing...
1. In the structure of the antibiotic Aztreonam illustrated below, how many nitrogen atoms have a sp2 hybridization state? 2. What is the number of oxygen atoms on which the negative charge will resonate by following relevant resonance structures? (0,1,2,3,4 or 5) 3. Identify the stereochemistry of each of these double bonds marked 1 and 2 in the structure below ((E) or (Z)) 4. What is the absolute configuration of the following molecule? (R/S) 5. Determine the relationship between these...
I have completed some answers! I just really really need help with the rest! I am so lost! please help me, if you can! What information do you need? Can you see the pictures that I posted? #2-6 are using the FIGURE from question #2 #7-8 go together and uses #7 FIGURE #9-12 uses #9"s FIGURE but #11 and #12 compares the two FIGURES from #7	 #13 and 14 are together # 15 and # 16 are their own problems...
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 in multiple choice format What is the relationship between these two 23. What is the relationship between these two molecules? molecules? BH BH que a. identical b. enantiomers c. diastereomers d. constitutional isomers 19. Which statement is FALSE about chiral molecules? a. Their chiral Carbons are sp hybridized. b. They have an internal plane of symmetry. c. They are optically active. d. Chiral centers are bonded to four different groups. a. enantiomers b. diastereomers c. identical d. unrelated...
MULTIPLE CHOICE (4 points each) Chow - III IV Use the Fischer projections above to answer questions 1-4 1) Which of the following pairs represent enantiomers? a) I & II b) I & III c) II & IV d) I & V e) II & V 2) Which statement is TRUE about I & IV? a) They are enantiomers. b) They are diastereomers. c) They are the same. d) They are not isomers. e) They represent a meso structure. 3)...
1. Consider the three molecules below to answer the following questions. Circle TRUE or FALSE at the end of each question (0.5 points each). Molecule A Molecule C Molecule B A. The rate of EAS with Molecule B will be faster than the rate of EAS with Molecule A (assume MAJOR product formation). TRUE or FALSE B. Molecule C will undergo nitration to yield a meta-product that is the MAJOR product. TRUE or FALSE c. The rate of meta-product formation...
3/4 d) Draw the structure of the MINOR product below. No mechanism needed here. (2 pts) 7) Draw the mechanism of the elimination reaction below (6 pts) EN (1 pt) b) What is the name of the specific mechanism of the reaction? c) What is being eliminated in the reaction? (2 pts) 8) A molecule in the conformation shown below undergoes the same type of elimination reaction as the previous problem. Draw the product of the reaction in full line...
I need some help to answer these following questions. Thanks. 41. Which molecule(s) is/are aromatic? I1 IV (A) I only (C) I, III, and IV (B) I and IV (D) I, II, III, and IV OH OH 42. Which Fischer projection represents this structure? HO OH OH H CHO CHO (A) H-OH (B) HOH HOH CH2OH CH2OH CHO HOH CHO но -н CH2OH CH2OH 43. Which is a product of this ozonolysis reaction? 1.03 2. (CH3)2S H O I BHs/THF...
1. (18 points; 3 points each] Multiple Choice: Circle the best answer i. Consider the following reaction: Xooot THF, A If there are no other changes, what is the effect of doubling the concentration of the starting alcohol on the rate of this reaction? a. No change b. Doubles the rate C. Triples the rate d. Quadruples the rate ii. Which nitrogen compound below would react fastest as a nucleophile in an 5, 2 reaction? NH NH N d. "NH2...