デジタル形式で段階的に解決 ありがとう!! SOLVE STEP BY STEP IN DIGITAL FORMAT Write the products of the following reactions, if there is more than one product, enter them and indicate which is the majority and if the compounds present stereochemistry, it must be entered appropriately. EXPLAIN THE REACTION MECHANISM STEP BY STEP Br NaC N HO OH D HCI OH PBr 3 + Δ HCI, H₂O F
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- 7A Write the possible products of the following reactions, the mechanism by which they were formed. mentioning Br CH3OH CH3ONaPredict the product of the following organic reaction: CH₂ CH O || C–CH2–CH=CH—(CH2)3 CH3 (CH₂)3 CH=CH- - CH₂ CH3 + 4 H₂ Ni CH,−O -C–CH2–CH=CH–CH=CH–CH2–CH3 Specifically, in the drawing area below, draw the chemical structure of the product P. If there is no product, because this reaction won't happen, check the No reaction box under the drawing area. Click and drag to start drawing a structure. × Ś +人工知能を使用せず、 すべてを段階的にデジタル形式で解決してください。 ありがとう SOLVE STEP BY STEP IN DIGITAL FORMAT DON'T USE CHATGPT 3.- Provide the products of each reaction and say what type of product it corresponds to (SN1 or SN2). As well as the reaction mechanism from which they are formed. ゾ Br Na CN CH3CH2OH Na OCH₂CH3 EtOH
- Pericyclic Reactions: Convert 1a to 1b Indicate what type of reactions and mechanisms occured in each step. Indicate reagents/conditions.3) Fill in the red box(es) with the missing reactant(s), reagent(s), product(s), solvent, and/or conditions and write a reasonable mechanism for the reaction. Not every box needs to be used and not every box necessarily corresponds to only a single species. If no reaction occurs OR no reagents exist to perform the reaction state, “NOT POSSIBLE” AND explain why. H₂O*Methionine, C5H₁1NO2S, is an essential amino acid in humans that is important in angiogenesis and the growth of new blood vessels. When methionine is burned in the presence of excess oxygen, O2, what products are formed? Select all products formed. NO₂ S₂ CO₂ No answer text provided. N₂ H₂O SO2
- Peroxides are often added to free-radical reactions as initiators because the oxygen–oxygen bond cleaves homolytically rather easily. For example, the bond-dissociation enthalpy of the O¬O bond in hydrogen peroxide (H¬O¬O¬H) is only 213 kJ>mol (51 kcal>mol). Give a mechanism for the hydrogen peroxide-initiated reaction of cyclopentane with chlorine. The BDE for HO¬Cl is 210 kJ>mol (50 kcal>mol).b) Refer to the following equation to answer Q3b (i), (ii) and (iii). CH3 H,SO, Н—с—он C-CH3 ? + H2O Но- ČH3 (i) Determine the product of the above reaction. (ii) Name the above reaction. (iii) Propose the mechanism for the above reaction.Describe the reaction mechanism for the hydrolysis of 2-bromo-2-methylpropane [CH3C(CH3)2Br] with aqueous hydroxide ions (OH-).
- CH3 CH3 Br- Br2 CH2CI2 CH3 CH3 H3C H3C Br Electrophilic addition of bromine, Br2, to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH2C12. In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due to steric clashes, the bromide ion always attacks the carbon from the opposite face of the bromonium ion so that a product with anti stereochemistry is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions CH3 CH3 Br- .CH3 .CH3 H3C H3C :Br :Br:Predict the products and mechanisms of the following reactions. When more than oneproduct or mechanism is possible, explain which are most likely. isobutyl chloride + AgNO3 in ethanol>waterProvide reagents in the spaces provided for the following transformations. If there are multiple steps 7.) needed, then indicate with a 1./2., etc., as appropriate. In several instances, there is more than one right answer. ОН E Br F G В Br Br K al `Br Br м obtained from fossil fuels in the ground H. A H В K L F M G