In the Synthesis of 3,6-dimethyl heptanone, starting from acetoacetic ester, we need * the following reagent Base, acid, and alkylhalide and heating O Base, acid, and alkylgroup and heating Base, H20, and heating O
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Q: Write the reagents used to synthesise the following compound starting from the benzoic acid CH3 ?…
A: Since you have posted multiple questions, we are entitled to answer the first only.
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Q: Draw the organic products formed in attached reaction.
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Q: The main product was formed for the following reaction HO (R)-2-bromobutane 25 °C
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Q: 10:30 „. 86%| E AIATS For Two Year Medic. 77 /180 (02:54 hr min Mark for Review When ethyne is…
A: When the ethyne is heated with mercuric sulphate and dilute sulphuric acid at 333 K, vinyl alcohol…
Q: Draw the organic products formed in attached reaction
A: The organic products formed in attached reaction can be drawn as,
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Q: Draw the product of the reaction shown below. Ignore inorganic byproducts. Но OH H2SO4
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A: Ethanol under oxidative condition produces acetic acid.
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A: 2-butanone undergoes catalytic hydrogenation to produce 2-butanol.
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A: Answer given as follows
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A: The hydrolysis reaction taking place is given as,
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A: Hello dear, Compound 8 is more reactive.
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A: LiAlH4 reduces carboxylic acid so as to form corresponding alcohol.
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Q: The main product was formed for the following reaction * HO (R)-2-bromobutane 25 °C
A: We are to predict the product formed when (R)-2-bromobutane reacts with OH– at 25°C
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Q: Draw the products formed in attached reaction.
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A: TsCl convert alcohol into good leaving group.
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A: The reactions taking place are,
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A: To choose: The correct option for acid catalyzed hydration of aldehyde and ketone by acid.
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A: The ester prepared is given as,
Q: Draw the structure of the major organic product(s) of the reaction. CH30. H20 CH3Ó • You do not have…
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Q: Draw the structures of the neutral organic products formed in the following reaction. Do not draw…
A: Please find below the mechanism for the reaction taking place.
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- 22. Provide the following: 1) the major organic product of each reaction shown, and ii) the specific name of the reaction in the first step. aniline AICI (if o,p-substituted products are possible, only provide the major para-substituted product, otherwise, only provide the meta-substituted product) 12, HNO (if o,p-substituted products are possible, only provide the major para-substituted product, otherwise, only provide the meta-substituted product) end a chata) A specific example of the Curtius rearrangement of an acyl azide to an isocyanate. b) The anionic intermediate that undergoes rearrangement in the Hofmann rearrangement below. 2 equiv NaOH, „NH2 NH, Br, H20 CO2 c) The iminium ion that is reduced in the in the reductive amination below. d) The Michael addition adduct that is generated in the Robinson annulation below. catalytic NaOCH3, CH;OH H3C + H20 рH 45 A NABH;CN CH;ÓH1// In a set of the given reactions, acetic acid yielded a product C C6 H6 C HM9B CH;COOH + PCl, → A anh. AlCl ether What would be product C? 2// When propionic acid is treated with aqueous sodium bicarbonate formed? 3// When CH3COOH reacts with CH3-Mg-X formed? 4// What is the product in the given reaction when benzyl chloride reacts with benzen?
- Give the major product of the following reaction. NaOH H* ? -CI heatExplain why pentane-2,4-dione forms two different alkylation products (Aor B) when the number of equivalents of base is increased from one totwo.Synthesize 2-methylbutanoic acid from 2-methylbutene. Please provide all steps and reagents used.
- A Give the main organic product that would form after the following reaction. OMe OMe H₂O H* IThe final products for the hydroxide-ion-promoted hydrolysis of an ester re the carboxylate ion and methanol instead of the carboxylic acid and methoxide ion. Why?b) The Wolf-Kishner reduction is a reaction used in Organic Chemistry to convert carbonyl functionalities into methylene group. The reaction was used to convert an aldehyde or ketone to an alkane using hydrazine, base and thermal conditions. The mechanism begins with the attack of hydrazine of the aldehyde or ketone. Stage 1: The reaction of aldehyde/ketone with hydrazine to produce hydrazine Stage 2: Reaction with the base and heat to convert hydrozone to alkane Write the mechanism of the reaction.
- In biochemical reactions, decarboxylation of carboxylic acids typically takes place for-keto carboxylic acids. Justify a rational why nature opted for-keto carboxylic acid decarboxylation. Among the following types of biochemical reactions, ester hydrolysis, rearrangement reactions, water elimination reactions, and anhydride hydrolyses, which one is the most favorable one. Rank the above reactions types in the order of being the most to least favorable reaction3-Hexanone can be synthesized from butanal and ethane using a Grignard reaction. The first step must be O creation of a carbocation O protonation of an oxygen nucleophilic attack of the aldehyde free radical halogenation preparation of an acetylideDefine the following reagents or functional groups as being related to either aldehydes/ketone AK, carboxylic acid derivatives CA or both. Imines Acid anhydrides Hemiacetal Aldol i) LIAIH4 ii) H+, H20 Haloform