Propose a one-step synthetic route to obtain 1-octyne from sodium acetylide.

Q: Please help me find the reagents of the synthesis

A: To solve this problem we have to do following steps (1) alkyne is treated with NaNH2 to form a ionic…

Q: the

A: The reaction is very well termed as acid catalyzed hydrolysis of a ketone to form a cyclic acetal.…

Q: 1. Propose a synthetic route for the desired products. a. b. &=&m OH OH HO CH3 OH

A:

Q: 3. Devise a synthetic strategy to complete the following transformation. ОН a. Retrosynthetic…

A:

Q: Design a stepwise synthesis to convert cyclopentanone and 4-bromobutanal to hydroxyl aldehyde A.

A:

Q: Which combination of reagent is appropriate for the following transformation? Ph OMe Ph HO.

A: Given transformation is,

Q: Draw the missing organic structures in this short synthetic sequence. Assume an appropriate workup…

A:

Q: NaOH

A:

Q: Provide a detailed arrow-pushing mechanism for the following transformation: Me PHOH PhO. Et Мe Me…

A:

Q: "Using retrosynthetic analysis, provide a synthesis for the fölloWIng reagents next to the arrows…

A: Synthesis: amine fragment can be synthesized from Gabriel synthesis. Acid fragment can be…

Q: Find a synthesis route for the transformation below Br

A: In this question, we will synthesized the final organic product from the starting material by using…

Q: 1.What is the best reagent to complete this synthesis? OA 1)???? CN 7.) NaCN.

A: Since you have posted a multiple questions in a single session, we are entitled to answer first…

Q: Chemistry Help woth this three retrosynthesis. thank you Provide a retrosynthesis and a forward…

A: TM 1 : Epoxide opened with 1-napthol. TM 2 : see below. TM 3 : Ethyl benzoate is subjected to Fridel…

Q: Propose an efficient synthesis process for this transformation. HO,

A: Williamson Ether Synthesis: Williamson ether synthesis is a type of coupling reaction for the…

Q: Which of the following alcohol/s would react to Lucas reagent after: <6 min 1-5 min <1 min

A: Tertiary alcohol reacts instantly with Lucas reagent. Secondary alcohol reacts within 3-5 min.…

Q: Devise a 4-step synthesis of the product from the starting material. CH3 1. reagent 1 2. reagent 2…

A:

Q: Starting material multi-step synthesis?

A: The synthesis given is,

Q: 6 Show how to synthetize the following target: (a)

A: Organic reaction mechanisms.

Q: Place reagent combinations in the out to successfully carry the following transformation. ? Ph Ph…

A: Lithium aluminium hydride is strong reducing agent...it reduces azide into primary amine..... R-N3…

Q: show and explain the mechanism with 3-nonenoic acid to y-nonanoic lactone?

A: The reaction of the conversion of 3-nonenoic acid to nonanoic lactone is the conversion of a…

Q: Show how to convert each starting material into benzylamine in good yield

A:

Q: Give a reduction that you can use to synthesize benzaldehyde.

A:

Q: Show how to convert each starting material into benzylamine in good yield

A: Given starting material,

Q: MeH Ме ОН N. H. Fill in the necessary reagents to complete the given reaction.

A: Reaction 1 : At ring junction methyl and hydrogen are trans. In the product Me and H are opposite…

Q: Propose a synthetic route for the following conversion: N. toluene benzyl (methyl) amine

A: Stepwise reaction answered below.

Q: He OH et worle HO

A: An acetal is a compound that has two ether-like -OR groups bonded to the same carbon atom of what…

Q: Propose a mechanism for attached reaction:

A: In this reaction, 'O' gets protonated to alcohol followed by the delocalization and the attack of…

Q: 3. Devise a synthetic strategy to complete the following transformation. a. Retrosynthetic analysis…

A:

Q: 19. Show how 4-methyl-3-hexanol can be synthesized from 3-pentanone.

A:

Q: Propose a synthetic route for the following transformation: ?

A: Alkenes are species which readily reacts with electrophile.

Q: . Williamson Ether Synthesis Questions for lab , Synthesize phenacetin from acetaminophen (Tylenol)…

A: Applying concept of Williamson Ether Synthesis.

Q: Propose an efficient synthesis process for this transformation. HO HO

A: Given reaction,

Q: What is the best choice of reagent(s) to perform the following transformation?

A: In this question stereo chemistry have not mentioned to the given product. so it should be Br2 CCl4

Q: Starting with cyclohexanone and ethanol as the only organic reagents, use any inorganic reagents to…

A:

Q: Propose a synthesis for each of the Target Molecules below. You may use any reagents you wish, but…

A:

Q: Propose a synthetic route to the indicated product: ÓH

A: -COCH3 group is electron withdrawing group.  Thus it is meta directing group for electrophilic…

Q: Ph OMe Ph HO

A: Given transformation is,

Q: Br -F (a) OH (h) CI CI (c) d)

A:

Q: draw the product

A:

Q: Give a reaction you could use to convert Benjamin to aniline

A: Organic reaction mechanisms conversation of benzene into aniline.

Q: Specify the reagent you would use in each step of the following synthesis: CI step 1 step 2 H.…

A:

Q: ăzidé âñd á third pathway using Gabriel synthesis) b. Starting reagent: 2-phenlethanal (Show two…

A: The question is based on the concept of organic reactions.   We have to convert the reactant into…

Q: DH

A:

Q: Devise a synthesis for the following transformation. SM = starting material. TM = target molecule Br…

A: We have to perform the transformation:

Q: Show the product of treating y-butyrolactone with reagent.

A: The product of gamma-butyrolactone with the given reagent should be shown.

Q: Propose a synthesis of the following target compound starting from benzonitrile. Remember to start…

A: Benzonitrile is first fluorinated then reduced to give benzyl amine which was then alkylated.

Q: OH

A: 1.Diethyl malonate is first alkylated using methyl bromide and sodium ethoxide. Second alkylation…

Q: Br NaOH heat Draw E1 Major Product + Draw Minor E1 Product

A:

Q: 16. HO OH 17.

A: Given are organic synthesis reactions.