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4 pts Question 3 Provide the names of the functional groups in this molecule. CH3CH2 CH3CH,...
(3 pts) Provide 2 acceptable names for the molecule below. If you provide a systematic name, include the appropriate R or S designation in the name. (2 pts) Provide a systematic name for the molecule below. (2 pts) Indicate whether the listed solvent is protic or aprotic. a. tert-butanol [(CH3)3COH] b. formamide (HCONH2]
S pts 2. Determine the chemical formula and identify the functional groups for the following molecule: HN 6 pts 3. Name the following molecule: Y Y 3. 7,8 - Dimethyl-4 propan-y-ylnona
Question 3 (1 point) Which functional group is found in this molecule? Alcohol Aldehyde Ketone Carboxylic Acid Question 4 (1 point) Which functional group is found in this molecule? LCHE HE-CH2-CH-CH3 H.COM Alcohol Aldehyde Ketone Carboxylic Acid Question 5 (1 point) Which functional group is found in this molecule? CH2-CH3 Alcohol Aldehyde Ketone Carboxylic Acid Question 6 (1 point) Which functional group is found in this molecule? CH,CH,CCHCH2CH.CH CH Alcohol Aldehyde Ketone Carboxylic Acid Question 7 (1 point) Which functional...
1. (3 pts) Provide 2 acceptable names for the molecule below. If you provide a systematic name, include the appropriate R or S designation in the name.
Problem #3 Provide full IUPAC names for each molecule below: a) a) e ii Hgc CH₂ H₃ C CH Problem #4 Draw the major product expected from each reaction below. HS HOOH SH, H+ 2. Raney Ni нс CH3 P-TSOH CHE H₃C 5 NH₂ 1. NHANH 2. KOH, AA pH - 5 pH
answer (3 pts) 4 of 6 7. Label all functional groups present within the following molecules. Ifa higher priority functional group is comprised of two or more other functional groups, label the higher priority group only. (2 pts each) OH penicillin 8. Which of the following compounds is/are optically active? Circle your answer. (2 pts each) meso-tartaric acid L-cysteine 1.4-butanediol (R)-2-iodohexane 9. Rank the following in order of increasing acidity. (5 pts) HF CH3NH2 CH3OH HB CH3CH2CH2CH2CH3
4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Me NH но HK он 1 4 5. 6. 3. 2. NH2 O) 08 4. (3 pts) Using retrosynthetic analysis, provide a synthesis for the following molecule. Place the required reagents next to the arrows and the necessary intermediate in the box provided. Me NH но HK он 1 4 5....
phone to complete the task. Question 1 4 pts Use ChemSketch or ChemDraw software (or hand drawn) to provide the correct structure of the product of the reaction below. Br2 --> Upload Choose a File 6 pts Question 2 12:01 PM Fri Jul 24 92, Et Question 2 6 pts Based on your lab report, which of the following compounds will de-colorize bromine solution in less than 1 minute? a) Cyclopentane b) 2-Methylbutane c) 2-Pentene d) Benzene e) 3-Methylcyclohexene f)...
Question 12 12 pts Provide an appropriate name (IUPAC or common) for the molecule shown. BIVA-A-I EX 3 1 1 * x, EE ? V T TH 12pt Paragraph
Please answer number 4 Question 3 1 pts Let us introduce a second person, who has standard Cobb-Douglas utility ug = (x+3). (x?). Their endowments are wa = (6, 3) and W3 = (3,6). You may assume p2 = 3p. Find the amount person A consumes of good 1 in competitive equilibrium. Simplify decimals (no extra zeros). Question 4 1 pts Find the contract curve (the set of all Pareto efficient points) for the setting in question 3. BIU A...