MgBr Me 1. Et20 Me + (1) 2. HCI 1. Et20 + (2) MgBr 2. HСI OH MgBr 1. Et20 2 equiv. + (3) 2. HСI List of electrophiles: D20 NaOD OMe HO. H i) ii) iii) iv) v) vi) vii) O=
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- Chemistry please provide the flow of electrons aswell!! thank you! using the starting material (on the left) to determine the sythetic route which will be the most reaosnable and effective to theres none, you have to start witth the begin products to get to finish needed by using the minmium reagents and reactions needed to get to the final productThe name for Reaction 1 is _____ while Reaction 2 is called _____. Choices: A. Williamson Ether synthesis, B. Hydration, C. Epoxidation, D. Acidic cleavage The reagent/s for REACTION 1 is/are ______ Choices: A. m-chloroperoxybenzoic acid, B. H2O/H3PO4, C. H3O+, D. HI The reagent/s for REACTION 2 is/are ______ Choices: A. m-chloroperoxybenzoic acid, B. water in acidic medium, C. dilute acid, D. hydroiodic acidSupply the missing reagent in the following reaction: (see attachment) A. Lindlar, H2, mCPBA B. O3 or KMnO4 C. fused KOH D. NH3 E. NaNH2
- For butenafine, develop a synthesis that starts with napthalene and benzene. (aromatic methyl groups can be converted to alkyl bromides using Br2/light, and aldehydes by heating the alkyl bromide in DMSO, eg. ArCH3 to ArCH2Br then to ArCHO).Provide a retrosynthesis (with complete reaction conditions) of the followingcompound from alkyl halides containing 6 carbons or less. The starting materials may be any type of alkyl halide (primary, secondary, or tertiary). You may use any other reagents you find necessary.Give the major organic product of each reaction of γ‑valerolactone with each of the given six reagents under the conditions indicated. Do not draw any byproducts formed. Reagent 1. NaOH, H2O, heat, then H+, H2O 2. (CH3)2CHCH2CH2OH (excess), H+ 3. (CH3CH2)2NH and heat 4. CH3MgI (excess), ether, then H+/H2O 5. LiAlH4, ether, then H+/H2O 6. DIBAL, toluene, low temperature, then H+/H2O
- Show how to prepare each alkyne from the given starting material. In part (c), D indicates deuterium. Deuterium-containing reagents such as BD3, D2O, and CH3COOD are available commercially.Fill in the missing reagents below.Propose a short synthesis f or ONE of the following molecules. You can start with acetylene, and alkyl halides from 1-4 carbons in length. You can also use an reagents you wish. a) Hexan-3-one (CH3CH2COCH2CH2CH3)
- What are the various functions of phenolics and Give seperately industrial uses of phenolics. Answer two pagesShow how to make these deuterium-labeled compounds, using CD3MgBr and D2O as your sources of deuterium, and anynon-deuterated starting materials you wish. CD3CH2CH2OHCould you please help me with this question I am very stuck. Give the major organic product of each reaction of methyl pentanoate with the given 6 reagents under the conditions shown. Do not draw any byproducts formed. (see photo) a. Reaction with NaOH,H2O heat; then H+,H2O b. Reaction with (CH3)2CHCH2CH2OH(excess), H+ c. Reaction with (CH3CH2)2NH and heat. d. Reaction with CH3MgI(excess), ether; then H+/H2O e. Reaction with LiAlH4, ether; then H+/H2O f. Reaction with DIBAL (diisobutylaluminum hydride), toluene, low temperature; then H+/H2O