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- 4) Draw both the intermediate product and the final product of this sequence of reactions - assume no carbocation rearrangements ( H-C=C-H Br₂ 1 equivalent Final Product Intermediate Product H₂ Gas (excess) Pd/C5. What is the major product of the following reaction? OH A) I B) || C) III D) all of the above E) none of the above H₂SO4 heat ||| LOSO3H10-) What are the major products of the following reactions? H H20 1.) Hg(OAc),, THF-H,O 2.) NaBH4 OH 1-) BH3-THF 2-) H,О, ОН
- 6) For the following Syl reaction: Draw a full 3-step mechanism with electron flow, intermediates, and the final product(s). excess CH₂OH 45 °CMechanism: A reaction mechanism for the following reaction is shown below. H+ CEN CEN: N-H || -C-OH H₂O, H* Step 1 wand woled mot ozsm E Step 3 N-H C-OH C=N-H Step2 C=N-H H-O-H H₂O motno vgiene fesrigid onlt to smotnos -C=N-H a) The overall reaction is an example of b) Step 1 is c) Step 3 is d) Draw in the curved arrows for each step. e) Identify the nucleophiles and electrophiles where appropriate. f) Fill in the reaction energy diagram. H₂O: rate determining step to noipojovo hamwell sit 5(emise erit voittons 10) vanas mi sdgin al rainW di of E^ reaction progress →14. What is the product of the reaction shown below? Br NaCN H2O, H* DMSO heat ČH;Br CO,H Br A) B) CH;CO,H ČHĄCO,H ÇO,H Br CO,H D) ČH,Br ČH-Br
- What is the major product of the reaction below? What is the mechanism? ROH 1.png H,SO, heat A 2-methyl-2-butene, dehydration B 3-methyl-2-butene, dehydration 2-methyl-3-butanone, oxidation 3-methyl-2-butanone, oxidationH12.7 Unanswered • 3 attempts left What is the major product formed in the following reaction? А 1. В 2. C D 4. major product dilute H,SO, OH OH OH oso,H 4) 3.Complete the following reactions by identifying the major product(s) or the missing reaction conditions. No mechanism is needed. a) PCC OH HO CH₂Cl2 no necessary reagents for this equilibrium b) c) Hg(OAc)2 H₂SO4, H₂O
- Reactions Mechanism Major Product Mechanism Minor Product (SN1, SN1, E1, E2) (SN1, Sn1, E1, E2) t-BUOK t-BUOH, 50°C Br CH,CO, CH;CO,H, 50°C 3-Chloropentane 25°C (S)-3-Bromo-3-methylhexane - MeOHPropose a curved-arrow mechanism to show how ozone (O3) reacts with a carbon-carbon double bond to form a molozonide, the first intermediate in ozonolysis.122. For the following three step conversion of A to B, the appropriate sequence of reactions is A OH CAREER ENDEAVOUR B CHO (a) MnO₂; (CH₂OH),/p-TSA; PCC (b) PCC; MnO₂; (CH₂OH)₂/p-TSA; (c) PCC; (CH₂OH)₂/p-TSA; Jones' reagent (d) Jones' reagent; (CH₂OH)₂/p-TSA; MnO₂.