1. Name the following compounds: ОН o plan 2. Draw the steps of the mechanism for...
Provide a step-by-step mechanism to account for the product of
each of the following reactions. Show the structure of each of the
intermediates and use curved arrows to indicate electron flow in
each of these steps.
3. Provide a step-by-step mechanism to account for the product of each of the following reactions. Show the structure of each of the intermediates and use curved arrows to indicate electron flow in each of these steps. a) NaOEt (1 equiv) EtOH O OH...
Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: kad ОН H2SO4 Part 1: o= + O 0 HSO4 HO 120+ H2SO4 -OH n= 0 view structure view structure Part 2 out of 3 I он,о* Фо: о но" — I + он,0 finish structure ... draw structure ... Screen Shot 2019-11-13 at 6 3 attempts left Check my work Next part
1. Name the following compounds: b. C. Cl Cl он 2. Draw the following compounds: a. Z-2-bromo-2-pentene b. Trans-3-heptene c. 3-chloro-4-methylcyclopentene 3. Predict the major products and show the mechanisms: он H2SO4, heat
65. Draw the product of the following dehydration reaction. H2SO4 OH Ans: 68. Draw the mechanism for the following dehydration. LOH H2SO4 Ans: 71. Draw an energy diagram for the following reaction, assuming that it is exothermic. OH H2SO4 Ans: 73. What are the steps of arrow pushing involved in the following mechanism? ОН H2SO4 Ans:
1. Name the following compounds Br Br OH 2. Draw three benzene isomers with molecular formula CsHl4Br2. Name each of the three somers.
Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: LOH H,SO Part 1 out of 4 A. SO2 B. H2SO4 c. H20 finish structure ... D. HSO4 3 attempts left Check my work Next part What is the major organic product obtained from the following sequence of reactions? OH PBrg CN Multiple Choice (+)-2-Methylpentanenitrile O trans-2-Butene O (R)-2-Methylpentanenitrile O (9)-2-Methylpentanenitrile O
1. Give the IUPAC name for each of the following compounds. (2 pts each 8 pts total) OH ОН o que 2. Show the product and the mechanism for the following reaction (4 pts) [H) 2 тон
1) Name the following carboxylic acids (use both IUPAC and common names): ОН ОН (b) (c) ОН ОН (d) Br ОН ОН NH2 2) Draw the condensed and line structures for the following compounds (a) 3,4-dimethylhexanoic acid (b) Phenylacetic acid (c) 3,4-dinitrobenzoic acid (d) 2,2,3-triflurobutanoic acid (e) 3-hydroxybutanoic acid (1) o-hydroxybenzoic acid (g) a-aminopropionic acid 3) Name the following dicarboxylic acids (use both IUPAC and common names) Он (а) НО ОН НО. (b) он ОН ОН (d) ОН он ОН...
I need help determining the reagents needed for these
reactions.
Part 5. Draw the mechanism. Draw the mechanism for each of the following reactions shown below. Be sure to show all steps in the reaction, the intermediates formed at each step, and use curved arrows to track the flow of electrons (20 pts) H2SO4 OH H6-3-sit GO Draw your mechanism below: 4 o Acid so ontsler deprotonation first step 12 000 BP2 + HBO Draw your mechanism below: +HBO, +H-Br
Draw the products for the following reactions first assuming they occur by an SN1 mechanism and then for an SN2 mechanism. 2. 0-Na -00 OH () Br +NaOH H-O-Na ? (iii) ulll OH +NaOH Нас" CH3 (v) CН3З CH0NA ? +NaOCHs