Q: CH3 NaOCH3 CH;OH II
A: Biomolecular elimination (E2) reaction:E2 reaction involves a one-step mechanism in which…
Q: What reagent should be used to carry out the following reaction?
A: The reagent that can be used to carry out the above process is written as follows:
Q: Which of the following reactions does not give the carbonyl product shown? a. Which of the reactions…
A: Carbonyl group chemistry is the most important chemistry in organic synthesis. There are some…
Q: . (a) Oxidation of 1-butanol with PCC will produce which of the following? 2-chlorobutanal…
A: PCC oxidation and Williamson ether synthesis
Q: What starting materials or reagents are best used to carry out the following reaction?
A: This transformation can be achieved by Friedel-Crafts alkylation. But, Friedel-Crafts alkyaltion…
Q: Identify the best reagents to complete the following reaction.
A: Aldehyde functional group is -CHO , ketone functional group is RCOR Aldehyde and ketone both…
Q: In the synthesis of 2-methyl-pentan-2-ol from pentan-2-one, the source of the nucleophile in…
A:
Q: CH3 CH3 OEt NH3 A в D least reactive most reactive
A: Electrophilic aromatic substitution reaction takes place between the aromatic ring and electrophile…
Q: 8. Draw the major organic products of the following. 1) LDA 2) H `H 3) H20 large excess l2 NaOH 1)…
A: Carbonyl group is one of the important functional group in organic chemistry. The hydrogen present…
Q: Provide the reagents necessary to carry out the following conversion. OH 1. NaOCH3, 2. H30* а. Ob. O…
A: Here, elimination followed by hydration of alkene occurs following Markovnikov rule.
Q: Draw the product formed when phenylacetaldehyde (CsH;CH,CHO) is treated with each reagent.…
A: Since you have posted a question with multiple sub-parts, we will solve first three subparts for…
Q: of NaOH (а) H2O OCH3 (b) NH3 + OCH3 HCI (с) CH3CH2OH + OCH3
A: We have reaction of ester with NaOH , ammonia and ethanol.
Q: Which carbonyl group is least reactive for nucleophilic addition or substitution reactions? H2N II…
A: Give the following molecule.
Q: Rank the compounds in each group in order of increasing reactivity in nucleophilic acyl…
A: The rate of nucleophilic substitution increases if the compound has high electrophilicity.
Q: Draw the products formed when benzoyl chloride (C6H5COCl) is treated with each nucleophile: (a) H2O,…
A: a.
Q: Which reagent is required for this reaction? H. PPH3 PPH3 PPH3 PPH3
A: Aldehyde or ketone reacts with the triphenylphosphonium ylide to form an akene, known as the Witting…
Q: II AICI3 V 1) O3 II (H+], CH;NH2 NABH3CN (C10H12) 2) DMS (C3H1,0) (C10H15N) -H20 1) EtMgBr 2) H20 IV…
A: Details mechanism are shown in image. The IV compound is : 3-Phenylpentan-3-ol Hence the correct…
Q: Provide a synthesis of CH3CH2CH2 CH2 SH from any alkyl halide. Show the structure of all reactants…
A:
Q: D. What is the product of acid hydrolysis of the following ester with HCI CH,-CHC-O-CH-CH 1-CH3 a.…
A:
Q: Thiols or thiol (-SH) group is a better base than hydroxide (-OH) group in elimination reactions.
A:
Q: Which of the following is the best set of reagents that must be used to prepare (CH3)3COCH2CH3?…
A:
Q: What is the product resulted due to the reaction of 2-hydroxy-3-methoxybenzaldehyde with ethyl…
A: We have to give the products of the given reactions under basic condition.
Q: Draw the main organic product formed in each of the following reactions: (a) (b) (c) O + H₂O OCH3…
A:
Q: (a) Circle the two compounds that are not carboxylic acid derivatives. Circle only two. CONHCH NOH…
A: A. Carboxylic acid derivatives are : ester, amide, nitrile, anhydride, acid chloride etc. But…
Q: When this compound is combined with a trace amount of sulfuric acid and molecular sieves, which…
A: The correct answer is given below
Q: Which of the following starting materials and reagents would be best to produce 2-hexanol? a.…
A:
Q: a. Which of the following reactions does not give the carbonyl product shown?b. Which of the…
A: Since, you have posted a question with multiple sub-parts, we will solve first three subparts for…
Q: draw and complete the reaction: Carbondioxide reacts with very limited amount of…
A: The reaction given is in 3 steps as, 1) Carbondioxide reacts with very limited amount of…
Q: What reagent should be used to carry out the following reaction?
A: The reagent that should be used to carry out the above reaction is given below,
Q: Appropriate reagents to effect the following transformation is/are: H2N. 'reagents' NH NH O 1:4…
A: This is an example of F-moc deprotection that occurs under basic condition
Q: Among the choices shown, which reagents would lead to 3-pentanone from bromoethane? A 1L Cul 2)…
A: A. EtBr in presence of Li/CuI gives Et2CuLi which on reaction with EtOTs gives n-butane. B. EtBr on…
Q: What is the role of phosphoric acid in the synthesis of cyclohexene? it is an antioxidant that…
A:
Q: The carbonyl compound attacked by -C≡CCH3 to produce 3-hydroxy-3-methyl-hex-4-yne is _________.…
A: In the carbonyl compound the carbon has slight positive charge and oxygen has slight negative charge…
Q: Rank the compounds in each group in order of increasing reactivity in nucleophilic acyl…
A: Carboxylic acid derivatives undergo nucleophilic acyl substitutions on the carbonyl groups. The…
Q: What is an appropriate stepwise synthesis for 1-pentanol from butanal? NABH4/CH;OH; PB13; Mg/ether;…
A: 1) Last reaction reagent sequence is not correct because no solvent used with NaBH4 and no acidic…
Q: Which of the following reactions require ethereal solution? a. CH3CH=CH2 to CH3CH2CH3 b. CH3CH=CH2…
A: Among these reactions ; a) this conversion is possible when we do hydrogenation of the alkene.…
Q: Which of the following reagents is the best choice for oxidizing a primary alcohol to an aldehyde?…
A: Several oxidising and reducing agents are mentioned in the question and their activities to produce…
Q: Complete the synthesis of the following product from benzene and the given reagents. COOH CH3C1 KMnO…
A: The correct answer is given below
Q: Draw the structure of the product that is formed when the compound shown below is treated with the…
A: The given structure of reactant is 1-Bromobutane. NaCN is a good nucleophile .
Q: When synthesizing acetals and ketals, what is the main driving force behind whether the reaction…
A:
Q: Draw the products formed when D-altrose is treated with each reagent. a. (CH3)2CHOH, HCl b. NaBH4,…
A: Hi, since there are multiple sub-parts posted we will provide you with answers for the first four…
Q: stion 2 The reagent which converts a carbonyl group of a ketone into a e OCH3CH2CH2NHCH3; H3O+ O…
A: -> Carbonyl compound has electrophilic center which can give nucleophilic addition reaction to…
Q: H CH; CH;COOH A) H CH; HBr B) peroxides LCH; 1) BH3-THF C) 2) H.O NaOH
A: Solution- Answer is given below with structure and main product with the option wise;
Q: 1. (a) Oxidation of 1-butanol with PCC will produce which of the following? 2-chlorobutanal…
A: PCC is a oxidising agent. It's oxidise primary alcohol to aldehyde and secondary alcohol to ketone.…
Q: The following reagents/conditions are capable of selectively oxidizing a primary alcohol to an…
A:
Q: Indicate whether the compounds below undergo racemization when treated with aqueous acid or base.…
A:
Q: What reducing agent can selectively reduce aldehydes, but not esters? KMnO4 OsO4 LiAlH4 NaBH4
A: It is asked which reducing agent can selectively reduce aldehydes, but not esters. The options given…
Q: Draw the main organic product formed in each of the following reactions: NaOH (a) (b) + H₂O OCH 3…
A:
Q: Which of the following is NOT an efficient synthesis of 2-methyl-2-pentanol? 1) CH,MgBr (A) 2) Hо 1)…
A: The reaction which is not efficient for synthesis of 2-methyl-2-pentanol can be decided based on…
how to find the thiol that can be oxidized to produce propyl disulfide, CH3CH2CH2−S−S−CH2CH2CH3CH3CH2CH2−S−S−CH2CH2CH3.
Trending now
This is a popular solution!
Step by step
Solved in 2 steps with 2 images
- What is the best process for N-methyl pyrrole synthesis ?List the appropriate reagents that can be used in places with question marks in the following series of reactions.Write an equation for the reaction of CH2=CHCH2CH3 with each of the following reagents: a. Ozone, followed by Zn, H+ b. BH3 followed by H2O2, OH c. Bromine Can you write it out please and thank you
- Which of the following reducing agents will result to the formation of 3-hydroxypentanoic acid when reacted with 3-oxopentanoic acid? -- LiAlH4 -- NaBH4 -- H2/Pt -- H2/Linlar’s catalystUsing any necessary reagents, show how the following compounds could be prepared using ethylene oxide as one of the reactants: a. CH3CH2CH2CH2OH c. CH3CH2CH2CH2D b. CH3CH2CH2CH2Br d. CH3CH2CH2CH2CH2CH2OHSynthesising menthone is an exothermic process that includes a reflux procedure. Mark the correct statements. * A- The reflux process enables us to transfers energy to the reaction mixture for an extended period of time without loss of solvent or reagents. B- The reflux process increases the rate of the oxidation of menthol. C- The reflux process increases the yield of the oxidation of menthol. D- A water bath can be used in the preparation of menthone because the boiling point of the reaction mixture is below 100°C due to the inclusion of acetone in this mixture.
- What products will be obtained if the following compound is hydrolyzed completely in an aqueous solution of HCL?Which of the following method is the best method for the synthesis of hexanal A.) Method: Ozonolysis, Reactant: Ozone, Substrate: 1-cyclopentyl-1-hexene B.) Method: Reduction, Reactant: LiAlH₄, Substrate: hexanoic acid C.) Method: Oxidation, Reactant: H₂CrO₄, Substrate: hexanol D.) Method: Oxidation, Reactant: KMnO₄, Substrate: hexanol E.) None of the given choicesFill in the appropriate reagents for the following reaction:
- Predict the products resulting from vigorous oxidation of compound by H2CrO4.from compound 3 to 4, the nitro group in compound 3 is going through [ hydrolysis / reduction / substitution / oxidation] to afford compound 4Which of the following reactions require a metal catalyst? a CH3CH=CH2 to CH3CH2CH3 b CH3CH=CH2 to CH3CH2CH2Cl c CH3CH=CH2 to CH3CH2CH2-OH d CH3CH=CH2 to CH3CHBrCH2Br