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- KMnO4, warm, conc'd reacts with hept-1-ene to yield __________. CO2, hex-1-ene CO2, hexanoic acid Formic acid, pentanoic acid Ethanoic acid, pentanal Formic acid, hexanoneComplete the following reaction: Pb+2 + SO4 -2 ---------------OChem help with IUPAC names involving Ph and Bn The phenyl group (Ph-R, C6H5-R) can be formed by removing a hydrogen from benzene and attaching a substituent to where the hydrogen was removed. The benzyl group (abbv. Bn), similar to the phenyl group, is formed by manipulating the benzene ring. In the case of the benzyl group, it is formed by taking the phenyl group and adding a CH2 group to where the hydrogen was removed. Its molecular fragment can be written as C6H5CH2-R, PhCH2-R, or Bn-R. Please provide the IUPAC name for the following: (Ph)2CHC(CH3)2CC(CH2)3CH(Bn)CHO
- Oxidation of Butanol -1 in KMnO4/H+ will produce-------------. a.Butanoic Acid b.Butanal c.Pentanoic acid d.Butene -2Assuming a 56.8% yield, how kany ml of alkene is required to produce 22.5 mL of 2,3-dimethyl-2-butanol? MW of alkene: 84.16, d: 0.653 MW of 2,3-dimethy-2-butanol: 102.17, d:0.823Carbocation Rearrangement in the SN1 Reaction of 2° and 3° alcohols with HX ?
- 6. Identify the best reagent(s) for this reaction. (see attached screenshot). a. H2SO4, HgSO4, H2O b. 1. Disiamylborane, 2. HO–, H2O2 c. K2Cr2O7, H+ d. NaOCl e. H2, PdI have this task in organic chemistry (book: Brown's introduction to organic chemisty, global edition). Task 10:42. In (a) I have to tell what the funcion of K2CO3 is in step 1. Is it that CO32- take the hydrogen atom in 1-napthol? Will it then be a SN2 mechanism? In (b) I have to name the amine used in step 2 to form Propanolol. But I can't really find out how to come up with an amine that will make that reaction. Here are two pictures of the task:Identify the reagents needed to come up with the given compounds. Pls Separate the reagents with a comma and a space. (ex. HNO3, H2SO4). For a multi-step reaction, separate the reagents with a semi-colon. (ex. HNO3, H2SO4; CH3Cl, AlCl3) There should be 9 reagents
- How much cyclohexanone (MW=98.15, D=0.9478) will be formed with 100% conversion of cyclohexanol (MW=100.158, D=0.9624)?1. What type of reaction is occuring in step 3? (halogenation, hydrohalogenation, reduction, keto–enol tautomerism, dehydrohalogenation, acid-catalyzed hydration, base-catalyzed hydration) 2. Which reagent is necessary for step 3? (Br2, HBr, H2/Pt, NaNH2, H20/H2SO4/HgSO4)Complete the flowchart by drawing the resulting structures of each reaction. A. B. C. D. E. F. G. H. I.