PCC is a mild oxidising agent and oxidize the Alcohol to aldehyde.
CrO3 is a strong oxidizing agent and oxidize alkene to Carboxylic acid.
NBS is a selective brominating reagent at allylic and benzylic position.
Hydroboration oxidation by Anti-markonikoff rule gives less substitited alcohol.
Show how you would synthesize the following a n d beginning with 1-butene, Bromma and any...
9- Show how you would synthesize the following compound, beginning with 1-butene, Bromobenzene and any necessary additional reagents. More than one step is needed. 8 Br OH Bromobenzene, 1-Butene Show hew you weulel Syntfesige 4-Nonanone, begining witA 1-Butanol and any other non- oraanie reagents.(1-Butanol is the only Organic compeonn availabe)
1. Which Wittig reagent would be used to synthesize 2 CH-CH=P(CAH) CH=P(CHẠh. P(CH3)3 CH,CH,CH-P(CH3)3 IV 2. What is the correct IUPAC name for the following compound? 6 eye 3. What is the correct structure for 7-methyl-4-octanone? 3 4. The products, D and E, of the following reaction sequence, S "CN HCI HCN CH.NO H20 heat would be: CH2CH2CN CH,CH,MgBe HO E ? ether Show how you would synthesize the following compound, beginning with 1-butene, Bromobenzene and any necessary additional reagents....
Show how you would synthesize the following compound starting with acetylene and compounds containing no more than two carbon atoms as organic starting material. You may use any additional reagents you need Br H H Br
4. In each reaction show how you would synthesize the product from the reactant. Show the reagents, conditions, and the structures of any important intermediates along the way. Any organic reagent may be used, and more than one step may be used as well. Include mechanism (+-) H Br
1. 2. Show how you would synthesize benzylamine from each of these compounds, using the following available reagents More than one step may be required. Enter the letters of the reagents necessary, in the order that they are to be used. Do not separate the reagents with punctuation. OH CI Reagents Available (a) NH3 (b) excess NH3 (c) H*, A (d) SOCl2 (e) N3 (f) H2, Pd/C (g) LiAlH4 then H20 (h) NaOH (i) CO, H2, heat and pressure Previous...
Show how you would use Grignard syntheses to prepare the following alcohols from the indicated starting materials and any other necessary reagents. Draw the Grignard reagent and any other organic reagents needed. 11 RUVIUWI Constans i Pendulu Part F Show how you would use Grignard syntheses to prepare the following alcohols from the indicated starting materials and any other necessary reagents. Draw the Grignard reagent and any other organic reagents needed. ОН -C-CH CH, from C-OCH.CH Draw the molecules on...
4. Propose a synthesis to create 3,4-dimethyl-3-hexanol from 1-butene. You only need to show individual steps and reagents, you do not need to show mechanisms. You must use 1-butene as your ONLY source of carbon atoms. The convergent processes have been outlined for you. for STEP 1: Show how to synthesize butyl magnesium bromide from 1-butene (5 points): BrMg STEP 2: Show how to synthesize 2-butanone from 1-butene (5 points): STEP 3: What intermediate forms below and what reagent(s) will...
7. Synthesis Problem (15 points) Show how you would synthesize 3 of the 4 following compounds in one chemical reaction. You may use any starting material you wish and any organic and inorganic reagents. Clearly indicate which ones you want graded by circling the molecules н, осн, Br ОН
question 8: Starting with 1-butene, how would you synthesize the following? он 1-butene CN он он
Select the reagents you would use to synthesize the compound below from benzene. (More than one step is required. If no third step is needed, choose (none).) Reagents Available f. KMnO4, H20 g. H2, Pd/C h. SO3, H2SO4 i. NaOH, H2O a. Br2, FeBr3 b. Cl2, FeCl 0 d. CH3CI, AICl3 Br e. CH3COCI, AICl3 N-bromosuccinimide (NBS) ball & stick labels Step 1: Step 2 Step 3