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A: The major product of the following reaction is:
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A: The explanation is given below-
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A: Half life = 28.5 years
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Q: 6.Balance the given skeleton reaction: O2(g) + NO(g) + H₂O(l) → NO3¯¯(aq) + H+ (aq) A. 2,4,3,4,4 B.…
A: Given equation: O2(g) + NO(g) + H2O(l) -------> NO3-(aq) + H+(aq)
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A: We will carried out the following transformation as follows
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A: A galvanic (voltaic) cell consists of an inert platinum electrode in a solution containing 1.0 M1.0…
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Q: ionic compound NaCl CuS Nil₂ CrCl V₂03 cation Na 0 anion Cl
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Q: Propose a synthesis of the target molecule from the starting material(s) provided. Please be certain…
A: Step 1 : Hydrogenation. Step 2 : Secondary alcohol oxidation using PCC. Step 3 : acetylide addition…
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- In an aqueous solution containing sodium bicarbonate, aniline reacts quickly withbromine to give 2,4,6-tribromoaniline. Nitration of aniline requires very strong conditions,however, and the yields (mostly m-nitroaniline) are poor. *(c) Although nitration of aniline is slow and gives mostly meta substitution, nitrationof acetanilide (PhNHCOCH3) goes quickly and gives mostly para substitution. Useresonance forms to explain this difference in reactivity.1.does acetylsalicylic acid can hydrogen bond witha. itselfb.water2. determine the electrophilic and nucleophilic of acetylsalicylic acidDevise a synthesis of (E)-tetradec-11-enal, a sex pheromone of the spruce budworm, a pest that destroys r and spruce forests, from acetylene, Br(CH2)10OH, and any needed organic compounds or inorganic reagents.
- Tunicates are marine animals that are called "sea squirts" because when they are taken out of water, they tend to contract and expel seawater. Lepadiformine is a cytotoxic agent (toxic to cells) isolated from a marine tunicate. During a recent synthesis of lepadiformine, the investigators observed the formation of an interesting by-product (3) while treating diol 1 with a reagent similar in function to PBr3 (J. Org. Chem. 2012, 77, 3390–3400):9. Product of the reaction of nitrobenzene with sulfuric acid in the presence of oleum at 60 °C:a) o-nitro benzenesulfonic acidb) m-nitro benzenesulfonic acidc) p-nitro benzenesulfonic acidd) None of the above 10. Due to their ability to move through ducts or pipes, they are generally called fluids:a) Solidsb) Solid mixturesc) Gasesd) Liquids and gasesReaction of (CH3)3CCHO with (C6H5)3P=C(CH3)OCH3, followed bytreatment with aqueous acid, affords R (C7H14O). R has a strong absorption in its IR spectrum at 1717 cm−1 and three singlets in its 1H NMR spectrum at 1.02 (9 H), 2.13 (3 H), and 2.33 (2 H) ppm. What is thestructure of R?
- LDA/THF, 78°Clongrightarrow Predict the major product of the following a- halogenation/a - alkylation reactions under the given reaction conditions.select the most appropriate reagent(s) to effect the change. 1. Disiamylborane, 2. HO–, H2O, H2O2 H2, Pd K2Cr2O7, H+ NaOCl H2SO4, HgSO4Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the a position. Predict themajor products of the reactions of naphthalene with the following reagents.(a) HNO3, H2SO4
- Reaction of p-cresol with two equivalents of 2-methylprop-1-ene affordsBHT, a preservative with molecular formula C15H24O. BHT gives thefollowing 1H NMR spectral data: 1.4 (singlet, 18 H), 2.27 (singlet, 3 H), 5.0(singlet, 1 H), and 7.0 (singlet, 2 H) ppm. What is the structure of BHT?Draw a stepwise mechanism illustrating how it is formed.Devise a synthesis of (E)-tetradec-11-enal, a sex pheromone of the spruce budworm, a pest that destroys fir and spruce forests, from acetylene, Br(CH2)10OH, and any needed organic compounds or inorganic reagents.Capsaicin, the spicy component of hot peppers, can be prepared from amine X and acid chloride Y. Devise a synthesis of Y from (E)-6-methylhept-4-en-1-ol [(CH3)2CHCH=CH(CH2)3OH], CH2(CO2Et)2, and any required inorganic reagents.