Q: a) -СCH-CH-OH,-Br,-H, -CH-CHз b) -СООН, СООCH3,-CH-ОН,-ОН с) -СH-NHCH3,-CH-NHz-NHz,-CN
A: Answer:- This question is solved by using the simple concept of determination of priority order…
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A: Since you have asked multiple questions, we will solve first three questions for you. If you want…
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A: Iodoform test is used to detect the presence of carbonyl group.
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Q: b) он Ме Me H,C CH3 но
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A: BRONSTED-LOWRY THEORY OF CONJUGATE ACID/BASE According to this theory, when a base accepts a proton,…
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A: 1.The 1st compound contian -o-,this is ether group 2.second compound contain both halogen and acid…
Q: Question attached
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Q: 1) ? HO 2) CH3 CH2CH2C1 AICI3 CI- NaOH, 100 °C ? CH3 CH3 Ph H3C. Br ок O K* CH3 t-BUOH
A: Hey since you have posted a question with multiple sub-parts, we will solve first three sub-parts…
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A: The structures of the given compounds can be drawn as -
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Q: Draw the products of the following intramolecular reactions:
A: Since you have posted a question with multiple sub-parts, we will solve first three subparts for…
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A: We have to give the major products. The required products are shown below N.B.: Here in presence…
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A: Given reactant is phenol and product is salicylaldehyde. This is Reimer-Tiemann reaction.
Q: Label each stereogenic center as R or S.
A: Given,
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A: The reaction given is,
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Q: 1. CHзCH2MgBr excess d. CHCHCOCHЗ 2. Нзо" HCI е. + CH3OH
A: Applying concept of organic synthesis and readent.
Q: Name the following compounds: 1. 2. Br Hc-CH-CH-ö-OH 3. -CH-CH 4. H,C-CH-CH-OH CI 5. HC-C=C-CH,-CH,…
A: According to our policy we should solve one question (If any subparts present then we should solve…
Q: ОН HOH2C ОН ОН II CO2H CO2H Но- -H- H- -HO- HO HO- ČH2OH CH,OH II IV ÇO,H CO2H Но- H- H- -OH H- -OH…
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Q: ON OOH CN ÇHO -CH 3 OH CH3 CI
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Q: -CH2CONH2 1. Br2, NaOH
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Q: Convert each Haworth projection to its acyclic form.
A: Please find below the acyclic form of 1st Haworth projection.
Q: a. CH,CNHCH, + H;O* → ? + ? || · CH;CH,CH,C–OH + CH,NH, b. ? + H;O* c. CH,CHCH,CNHCH,CH; + ?…
A:
Q: Fill in the boxes
A: The reagents and the products are :
Q: MIG HBr, ROOR BAT Pool of Choices CH3 c JOH BIG cold dilute neutral KMnO4 CH3 Br IOH Br₂, H₂O PIG…
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Q: oper name for these compounds. Br OH OH Br a) b) CI c) CI CH3 Tevol (p H3C. CH3 H3C Br он
A: Given, Give the IUPAC names of the following compounds = ?
Q: CH,OH 38. CHCH,CH3 Br
A: We are authorised to solve only one question at a time. Please post rest of the questions…
Q: 7. ČH,CH, ČH,CH, CH 8. ČHa
A: As you not specified so I am giving answer of first three question as per guidlines Select the…
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Q: 6 S Cr₂O3 Base RX 4 KNO3 H₂SO4 carbonyl punodwoo HCI/Zn 2 3
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Q: NH EtO OEt H,N `NH2 starting materials
A: Answer is given below
Q: Fol (u) (v) (w) (y) i CI H + CH3NH₂ CH₂MgBr A Ph H₂NNH₂, OH Ph- Ph 1. HOCH₂CH₂CH₂OH, H* 2.CH3MgBr 3.…
A:
Q: (a) NaBD4 CH3CH,OH (b) NABH4 CH3CH,OD
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Q: CH,OH Br NaOH b. Br 1. Mg, diethyl ether d. HI ONa Br H,0 OH PBr,
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Q: 1. ВНз 2. NaOH, H2O2 A CHO HOʻ ÓH ОН OH B D HO A В O C о оо с
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Q: CO-CH, + 2 NAOH + CH,OH + H0 HO.
A: The question is based on the concept of organic reactions. we have to identify the product formed in…
Q: 1) (CHa),SICI / NEL CH 2) CH జ 1) 2) CH,CHICO,CH,CH, 3) H;0 (warm) 1) LINPI2 (LDA) /-78°C e) / 15…
A: We have to givemajor product of the following given reactions as follows in step 2:
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- Org. Chem. 1. EA26. Can you please draw out all four , and explain what a stereoisomer is in relation ? ThanksDraw the reactant RCHDBr with S absolute configuration, the draw the product of R’OH + RCHDBr (with S-configuration) through an SN2 reactions.Using chair confirmations, draw the final product of each molecule. Pls explain how are you arrived at the answerthank you!
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- In addition to organic halides, alkyl tosylates (R'OTs. Section 9.13) also react with organocuprates (R2CuLi) to form coupling products R – R'. When 2° alkyl tosylatee are used as starting materials (R2CHOTs), inversion of the conguration at a stereogenic center results. Keeping this in mind, draw the product formed when each compound is treated with (CH3)2CuLi.(a) Draw all stereoisomers formed by monochlorination of the cis and trans isomers of 1,2-dimethylcyclobutane drawn below. (b) How many constitutional isomers are formed in each reaction? (c) Label any pairs of enantiomers formed.Draw the reaction products for each SN1 reaction and indicate the appropriate stereochemistry.