10Starting with ethyl acetoacetate and formaldehyde as your ONLY sources of carbon atoms synthesize the following. The listed compounds are your only allowable sources of carbon! All other inorganic reagents and LDA are allowable. OH OCH2CH3
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- 4 Carry out the following synthesis (WITHOUT MECHANISMS) giving all the necessary reagents (reagents with their molecular formulas and products or intermediates with their structural formulas) for the following transformation:1-chloro-1-methylcyclohexane ------->6-hydroxy-6-methyloctanoyl chlorideDevise a synthesis of each of the following compounds. Besides inorganic reagents, you may use hydrocarbons and halides having ≤ 6 C′s, and CH2=CHCOOCH3 as starting materials. Each synthesis must use at least one of the carbon–carbon bond-forming reactions.Provide the major product(s) for each reaction below and you may assume there is anexcess of each reagent for each reaction
- Please help me with drawing following reaction steps.. Hydroboration 1-Hexene + (Diethyl ether as solvent + and BH3) -> Hexanol Alkene Bromination 2-Butene (Diethyl ether solvent ) + Br -> anti 2,3 Dibromo butaneSuggest the most appropriate method for each of the following laboratory syntheses. Ineach case, suggest both a chromium reagent and a chromium-free reagent. (a) butan@2@ol ¡ butan@2@one, CH3COCH2CH3(b) cyclopentanol ¡ 1-ethylcyclopentanol (two steps)Show how you would synthesize the following compounds, starting with benzene or toluene and any necessary acyclicreagents. Assume para is the major product (and separable from ortho) in ortho, para mixtures. 5-chloro-2-methylaniline
- In each case below select the synthetic procedure/s that could be used to carry out the transformation, giving the alcohol shown as the single major product.The procedures are:Hydroboration/oxidation: alkene + BH3; then H2O2, -OH.Oxymercuration: alkene + Hg(OAc)2, H2O; then NaBH4Draw structural formulas for the major product(s) formed by reaction of 3-hexyne with each of these reagents. (Where you predict no reaction, write NR.) Q.) H2O in H2SO4/HgSO4Propose suitable reagent(s) to accomplish the following transformations.
- Questão 10A certain hydrocarbon had the molecular formula C16H26 and contained two triple bonds. Ozonolysis resulted in CH3(CH2)4CO2H and HO2CCH2CH2CO2H as the only products. What is the reasonable structure for this hydrocarbon? Hexadec-6,10-dino undec-1,5-dino Hept-1,5-dino hex-1,5-dino nahhow how you would synthesize the following compounds, starting with benzene or toluene and any necessary acyclicreagents. Assume para is the major product (and separable from ortho) in ortho, para mixtures. 1-phenylpropan-2-olPlease help me with drawing following reaction steps.. Hydroboration 1-Hexene + (Diethyl ether as solvent + and BH3) -> Hexan Alkene Bromination 2-Butene (Diethyl ether solvent ) + Br -> anti 2,3 Dibromo butane oltane