Question 4 (1 point) Which of the following, when treated with Br, will yield the product...
Question 5 (1 point) What is the major organic product when the following compound is treated with Tollen's reagent?
11) Provide the structure of the major organic product which results when PhCH2CHO is treated with NaOH 12) Provide the structure of the aldol product that results when 4-methylpentanal is treated with sodium hydroxide. 13) What two molecules were condensed in an aldol reaction to produce (CH3)3CCH-CHCOCH3? 1-4) Predict the outcome of the follovwing reaction. 0 0 NaOH, heat 15) Provide the structure of the ester that would undergo self-condensation to yield the B- ketoester shown below.
1) Which base yields the most SN2 when treated with the same
starting material? (draw this structure with stereochemistry)
2)Which base would have the least yield of SN2?
3) What conclusions are made about the amount of SN2 product
formed as a function of base strength?
4) Discuss stereospecificity of an SN2 reaction and draw the
SN2 transition state intermediate formed when benzoate is treated
with starting material.
4. When the starting material shown below is treated with a variety...
QUESTION 1 For the following reaction, identify the 1,2-addition product. A) B) Br Br- Br + HBr C) D) Br ОООО С D 1 points QUESTION 2 Identify the product of the following reaction. + H,CO,C -CO,CH -CO,CH -CO_CH -CO,CH A CO,CH D) c) A) B) COACH CO,CH COCH, CO.CH B ОООО С D QUESTION 3 For (3E,5E)-octa-1,3,5,7-tetraene, shown below, how many of the a-molecular orbitals are bonding orbitals? 3 ОООО 6 PUS QUESTION 4 ОН ОН Which one of...
Question 4 0.6 / 1 point Which of the following compounds can probably be prepared in a good yield (as a major product) from benzene using two successive electrophilic substitution reactions? Check all that apply. Br CH G NO2 SOCH NO2 ii iv V iv Ov
Q 7.15: Which of the following dihalides would form an alkyne in the highest yield when treated with NaNH2? Br, Br Br Br
Draw the structure of the major product which results when the diene shown is treated with HBr at -80°C. CH3 CH3 Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. 1. H: 120 EXPONE H + с N o S CI Br Marvin JS 1 by ChemAxon P
Question 3 (1 point) What is the relationship between the following molecules? Br Br Same compound. Pair of enantiomers. Pair of diastereomers. Unrelated. Two of the above. Question 4 (1 point) Saved Which of the following molecules has stereogenic center with configurati Br estion 4 (1 point) ✓ Saved Which of the following molecules has stereogenic center with configuration R? Br o Br Question 5 (1 point) Which of the following is true regarding 50/50 mixture of the following molecules?...
Question 4: Starting with 2-methyl-1-propanol, draw the organic product formed when treated with the following reagents: OH 2-methyl-1-propanol a) H.SO,, heat HCI c) 1) TsCl, py PBr 2) NaSH
Question 2 (1 pt) When treated with aqueous NaOH, the following compounds give an aldol product which then undergoes dehydration to give a new product (with Estereochemistry). Please give structural formulas for both products. + TH + 1 H NaOH NaOH H20 + H₂O H20 Aldol product