Question

31 Multiple Choice Problems: 16 questions, 4 pts each =64 total. 1. Circle optically active molecules from the list below: HO

6. Below is hydrohalogenation reaction of alkene. Name the mechanism pattern in each step. Br Br H Br - Step 1: Less +2 protn

Sign of AH Sign of AS= 8. Rank the stability of those carbocations iii iv ii i 1 2-3<i

31 Multiple Choice Problems: 16 questions, 4 pts each =64 total. 1. Circle optically active molecules from the list below: HO Br H Br H HC 2. What is the relationship of the following two molecules, one in bond-line structure and one in Fischer projection? Br Me Me Cl CA Br Same molecule with same rotational conformation a. b. Same molecule with different rotational conformation C. Constitutional isomers d. Enantiomers Diastereomers e. Identify the resonance pattern for the following curved arrow(s) without giving the resonance structure. 3.
6. Below is hydrohalogenation reaction of alkene. Name the mechanism pattern in each step. Br Br H Br - Step 1: Less +2 protn tafe Step 2: Step 3: Auu atacks following elimination reaction:
Sign of AH Sign of AS= 8. Rank the stability of those carbocations iii iv ii i 1 2-3
0 0
Add a comment Improve this question Transcribed image text
Answer #1

1 Circle optically active molecules from the list below: LA OH HO 2 What is the relationship of the following two molecules,

Add a comment
Know the answer?
Add Answer to:
31 Multiple Choice Problems: 16 questions, 4 pts each =64 total. 1. Circle optically active molecules...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • please answer all Question 1 2 pts Determine whether the molecule below is optically active. cannot...

    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...

    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...

    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&#9 #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...

    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...

    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...

    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...

    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)...

    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...

    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...

    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...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT