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- (please answer all questions) 1) Predict the products from reaction of 1-hexyne with thesereagents: a) One equivalent HBr b) One equivalent Cl2 c) H2 , Lindar Catalyst d) NaNH2 in NH3 , then CH3BrI recovered 3 mL of water, how many grams of water was produced in the reaction please show how? Cyclohexanol can attack the carbocation intermediate formed during the synthesis of cyclohexene. Draw this side product with the molecular formula C12H22O.Could 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
- In the synthesis of methyl m-nitrobenzoate from methyl benzoate using HNO3 and H2SO4 via EAS the product is washed with ethanol to remove impurities. By impurities do they mean o-nitrobenzoate and methyl p-nitrobenzoate? How come ethanol can remove o-nitrobenzoate and methyl p-nitrobenzoate, but has no effect on m-nitrobenzoate? Thank you.redraw the following reaction mechanism with benzene instead of isoborneol. it's an oxidation mechanism from OH to ketone. please include the arrow pushing.QUESTION 4Predict the products(s) from the reaction of 1-hexyne with each of the following reagents:a) 1 mole of HBrb) H2O, H2SO4, HgSO4c) 2 moles of Br2d) Excess Cl2e) 2 moles of HCl with H2O2f) 1 mole of HCl
- (a) What happens when CH3—O—CH<sub3 is heated with HI?(b) Explain mechanism for hydration of acid catalyzed ethene :CH2 = CH2 + HzO CH3—CH,—OHEXP VIDEO https://www.youtube.com/watch?v=9Wxxv7kwXlA&list=PLE-217H0ao60Uzpzj-FNP_0ScVp5SZB7j&index=8 1.Pre lab question What are the functional groups in your substrate? -Nitrate -Nitrate and acetate -Amide and ether -Benzene ring b.The stable reaction intermediate in this reaction is Nitronium ion Benzonium ion Carbocation Carbanion c.How would you distinguish between 2-nitrophenacetin and 3-nitrophenacetin? -Color difference -Melting point difference -Difference in Molecular weight -They cannot be differentiated. dAn ether group is -Ortho para activating -Meta activating -Ortho para deactivating -ring activator eThe catalyst in this experiment was -Glacial acetic acid -Nitric acid -Sulfuric acid -Ethanol fThe chemical waste from this experiment should be discarded in the -Sink -Halogenated waste container -non-halogenated waste container -Heavy metal waste container. gWhat is the limiting reagent in this experiment? -Nitric acid -Glacial acetic acid -Phenacetin…Thank you for the answer, would it be possible to follow the path I have attached as well srarting from methanol ---> CH3Br -----> CH3MgBr-------> (H3C)CH-CH2OH ----> E1 Isobutalene
- Using 1-butyne, CH3CH2CH≡CH, write reaction steps to show how in the laboratory youmay prepare the following compounds. (No reaction mechanism is required)i) 1,1,2,2-Tetra chlorobutane (CH3CH2C(Cl2)CH(Cl2) ii) Butanal (butylaldehyde, CH3CH2CH2CHO)using any necessary reactants and reagents, propose reasonable syntheses of the following compounds from cyclohexanone can you please help with coumpound 3 (I attached it below). Thank you!Devise a synthesis of each of the following compounds. Besidesinorganic reagents, you may use hydrocarbons and halides having ≤ 6C′s, and CH2=CHCOOCH3 as starting materials. Each synthesis must use at least one of the carbon–carbon bond-forming reactions.
