10:20 PM Wed Nov 6Exam 2 Extra CreditINDEXCozort, Alexisล 24%04/4 answeredAnswers are saved automaticallyHand InAll your answers will automatically save as you proceed through the test.Saved==Question 3Fill in the Blanks1H"C(CH3)35H CH3Answers typed in all of the blanks will be automatically saved.x²2-Assign R or S configuration to the chirality centers in the molecule below.Carbon 1 configuration isWrite your response here...!Carbon 5 configuration isPlease type your answer to submitWrite your response here...Please type your answer to submitUnsaved: Please enter a valid answer:= Question 4☐

When four different groups are attached to an atom in such a way that the structure is non…

Answered: 10:20 PM Wed Nov 6 Exam 2 Extra Credit…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter13: Structure Determination: Nuclear Magnetic Resonance Spectroscopy

Section13.SE: Something Extra

Problem 39AP: Predict the splitting pattern for each kind of hydrogen in isopropyl propanoate, CH3CH2CO2CH(CH3)2.

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app:10Tack.co Type here to se OM C O Quin 23 of 30 A solution of a chiral compound was prepared by dissolving 15.67 g in 16.00 mL of solvent. The solution was placed in a tube that is 1.00 dm long. What is the specific rotation of light if the observed rotation was determined experimentally to be +62.41"? ✓ O 1 4 7 2 5 3 6 9 0 DAộ c * ▪ ✪ с x 100 1508227
Но LIGH + Cv (NO3)3 911₂0 ㅋ HH₂0, 120°C32904 24h ount B Used 0.839) - terephthalic and 09 Used 2,0g - Cr (103) 3 9H₂0
tps://app.101edu.co F2 910 # 3 + E F3 111 Compare the C-C bonds in the following structures: CH3-CH3, H₂C=CH2, HC=CH. Rank the C-C bonds in these structures in order from weakest to strongest. $ 4 R F4 ole in % 5 T Your Aktiv Learning trial expires on 05/23/23 at 12:59 AM F5 A) CH3-CH3 < H2C=CH2 < HC=CH B) HC=CH < CH3-CH3 < H2C=CH2 C) HC=CH
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BENZOIC ACID(Screenshot2113) : Find Bonds, Absoprtion Peaks [cm-1] and their functional groups (Alkane/Alyne/Alchol/Arene/etc..)
7. a) Identify all the chiral/stereogenic centres in the following molecules. Circle the chiral carbon(s). OH CI -Br CI ОН O,N CI Br CI CI A B OH HO, .CI Br HO OH b) For each chiral center, prioritize the groups (1-4) attached to each chiral center(s) Based on your priorities, assign R or S configurations to the chiral center(s). i) Но ii) H2N H ОН но OH iv) OH OH v) H,N- ČH,OH Draw the most stable chair conformation for each of the following cyclohexanes. Now, "flip" the ring and redraw the molecule in the higher energy form. i) chlorocyclohexane ii) cis-1-chloro-2-methylcyclohexane iii) trans-1-methyl-3-propylcyclohexane
TOPIC: POLARIMETRY INSTRUCTIONS: Solve for the observed optical rotation:
entify the configuration of each chiral center in the following compound: 5H 6F XX 10 11 In the boxes below, first input the number(s) corresponding to the chiral center(s) in numerical order as a comma separated list with no spaces (e.g., "1,3,4"). Then input the configuration(s) of the chiral center(s) in the same order and format (e.g., "R,S,S"). chiral center location(s): Configuration(s):
13.5: Ac xa overlap x || Dashbox Nearpo earpod.com/presentation?pin=BE1EF339D37FF<iLisResult=c67b6b Like previous example draw both chair con most stable chair. Instructions Me Br OH
match the IR spectrum

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