Can you please draw it and explain
Can you please draw it and explain Which of the following compounds is the product of...
can you please help for these three questions please? thank you! 18. Which will be the major product of the following E2 reaction? NaOH Br CH3 H3C H a) b) c) Нас d) H3C CH3 H3 H3C 3 20. Which would not be a good method to prepare compound A? O A 1. BH3 OH РСС b) 2. H202, OH 1, H+, H2O 2. РСС H2SO4, H20 O 28. How many different protons (including the H of the OH) are...
Hello! Just double checking the answers my organic chemistry study guide. Please go ahead and answer ALL the questions you see below, if you can't answer all then PLEASE let someone else do them! High rating only given to ALL questions complete 21. Provide reagents (including solvent and/or special conditions, such as light) to complete the following reaction scheme. CH3-CCH-CH2 CH3 H3C CO+Ho -CH CH OH Page 8 of 9 HC H3C gOCH2CH3 18. Draw the structure of the alkene...
Organic Chemistry please help asap 70. What nucleophiles wou cleophiles would form the following compounds as a result of reacting with l-iodobutane? OH SH 11. Draw (R)-2-bromopentane + CHO b. (R)-3-bromo-3-methylheptane + CH,OH c. benzyl chloride + CH CH OH te tollowing reactions: if the products can exist as stereoisomers, show what striscmers are obtained d. allyl chloride + CHOH e. 1-bromo-2-butene + CHO 1. l-bromo-2-butene + CH OH the products obtained from the solvolysis of each of the following...
10) Which one of the following correctly describes the reaction below? Draw the product СН3 H-+-Br NaSCHE ethanol water CH2CH3 Mechanism Rate Law A) SNI rate = k [(S)-2-bromobutane) Stereochemistry not stereospecific, but more inversion than retention of configuration B) Syl rate = k [(S)-2-bromobutane] [NSCH] stereospecific, retention of configuration C) SN? rate = k [(S)-2-bromobutane] not stereospecific, but more inversion than retention of configuration D) Sy? rate = k [(S)-2-bromobutane) [NSCH] stereospecific inversion of configuration
Draw the coupling product of the Pd(0)-catalyzed Suzuki reaction between the following compounds. Show the stereochemistry of the product. Show he stareog ermistry of the prooicaon between the folowing compounds. Draw the coupling product of the Pd(O)-catalyzed Suzuki reaction between the following compounds. Show the stereochemistry of the product. eproductatalyzed Suzuki H3C CH3 OH Pd(PPh,), Br CH2 CH2CH2OH
Махwell presented by Sapling Learning Draw the correct product for the following reaction. (If there is no reaction, draw the starting material.) K,Cr,O,/H,SO, ÓH Draw the major organic product(s) of the following reaction (multiple products may be drawn in one box): он HBr Classify the following transformation as a reduction, oxidation, or neither CH3 CH3 он Cна CH2 CH CH2 CH H3C Hас CH2 :0: reduction oxidation redox neutral
Name each of the following compounds, which contain a functional group. 3. Give the product for each reaction. For no reaction, write N.R. e. f. Br CH3 O HO Br g. CH3CH2NH2 + HCI [H] h. CH3CH2OH + CH3CH2CH2-C-OH [H] i. CH3CH2CH2CH2-C-OH + CH3NH2
What is the product of the following reaction? — н ннн н-с-с-С=С + H2O H,SO, Hн Hн ОН ОН ОН ОН What is the major product formed in the following reaction? сна 3 сні H,SO, Heat нас он 86 39 — 42 45 ОН ОН What product is formed in the following reaction? CH3 H3C-C-OH [O] CH3 No Reaction What product forms in the following reaction? 30 > 33 + HBT ✓ 36 Ono reaction 39 Br 42 45 Br...
1 9. Arrange the following in ng compounds in increasing (weakest to strongest) order of basicity. NH2 NH2 NO2 E. None of the above What is the product of the following sequence? 10. H3C CH3 OH он Na V. A I What is the major product for the following Reaction? 11. Pd(OAc)h PPhy Et N NO2 NO2 NO2 C.Ⅲ A. I D. IV V. 12. Predict the product for the following reaction. Br 1. NaNs 2. LiAIH4 3. H20 1...
please explain the work please explain the work 8. Consider isomeric compounds Y and Z: OTS H3C H3C, нс Сн, HECCH Z a. Draw the lowest-energy chair conformer of each isomer. b. Which compound would you expect to react at a faster rate in the E1 reaction? Briefly explain your answer. Hint: Think about the mechanism in terms of a reaction coordinate diagram. 9. Propose a synthesis for each of the following compounds using the indicated starting material. You may...