Draw a reasonable arrow - pushing mechanism that explains formation of the given products. Typo: on the last question, the product should have an ethyl group and not an alkene. HBr, A ㅇ Br ㅇ Br
Q: e w What is the product for the following alkylation? 1. NaOEt, EtOH, 25°C IV 2. Br oh
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A: the detailed mechanisms attached belowExplanation:
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Q: dont provide handwriiting solution ...
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A: we have to write best reagents to complete the following reaction
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- Which would be a secondary alcohol? . a) CH3 – CH2 – CH2OH b) CH3 – CH – CH3 OH c) CH3 – CH – CH2 OH OH d) OH CH3 – C – CH3 CH3 ODraw the structure(s) of the major organic product(s) of the following reaction. aqueous H,SO. KCNOE 2 O NH Draw the structure of all organic products formed in the following reaction. <-5 1. KOH 2. (CH₂)₂CHCH₂Cl 3. OH, H₂O
- Give the IUPAC name for the chemical in the attached image. [click on attachment to view image if you don't see it] CH3CH₂CH₂CH₂CHCH₂CH₂CH₂CH3 CH3CH₂CH₂ O A. 2,2,5,6-tetraethylhexane B. 2,2,5-triethyloctane O C. 3,6-diethyl-3-methylnonane CH₂CH3 D. 3-ethyl-3-methyl-6-propyldecane CH3When doing a dehydration, the product will have the __ (more/less) substituted alkene.Question 4. In the laboratory, reductions of carbonyl and carboxyl compounds are often carried out using reducing reagents, such as sodium borohydride (NaBH4) and lithium aluminum hydride (LiAlH4). While LiAlH4 can reduce aldehydes, ketones, and esters to the corresponding alcohols, NaBH4 cannot reduce esters. OH R `R'(H) alcohol no reaction 1) H Na+ H-B--H H 2) acidic 1) workup (H3O+) H Na* H-B™-H H 2) acidic workup (H3O+) R 'R'(H) aldehyde or ketone 1) NaBH4 2) acidic workup (H3O+) R OR' ester ملل 1) OEt H Li+ H-AI-H H 2) acidic 1) workup (H3O+) H Li+ H-AIH H 2) acidic workup (H3O+) OH 1) LIAIH4 2) acidic workup (H30+) R R'(H) a) Draw the products of reduction of the ß-ketoester shown below by NaBH4 and by LiAlH4. alcohol R OH + R'OH 1° alcohol b) Provide a rationale for why esters show decreased reactivity toward reduction by NaBH4, compared to aldehydes and ketones. c) Provide a rationale for the increased reactivity of LiAlH4 over NaBH4 that allows for the reduction of an ester.…
- Chemical Reactions: Give the product/s of each chemical reaction 1. Reaction of this alkene to the different reagents written above and below the arrows. ¡ HBr1. Give the IUPAC names for the following organic compounds. a) CH3CH2CH(CH3)COOH e) CH3CH(CH3)CHBRCOOH ) HOOCCH2CH(CH3)CH2COOH OH h) СООН СООН i) NO2 СООН j) O2N 9 ÇH2CH3 ÇH3 ? HOČCH,CHCH,CH,CHCH,COH k) CH;CH2CHCH,CH;CH3 1) ČO2HMacmillan Learning Consider the reaction between an alcohol and tosyl chloride, followed by a nucleophile. Write the condensed formula of the expected main organic product. CH₂CH₂CH₂OH 1. TsCl,pyridine 2. CH₂CH₂CH₂S CH,CH,CH,OS Incorrect
- You may want to reference (Pages 408 - 414) Section 12.3 while completing this problem. The compound frambinone has the taste of raspberries and has been used in weight loss. Its structure is HO |||-CH₂-CH, -C-CH3 ▾ Part A Identify the functional groups in frambinone. Check all that apply. ketone aromatic aldehyde ester ether phenol Submit Request Answer4> 39. This aldehyde is useful for its vanilla flavoring hence the trivial name, vanillin. A. B. 40. This important steroid hormone controls the development of male sex characteristics. Cortisone B. Testosterone C Progesterone D. Both B and C 41. The delighted odor of melted butter is attributed to this four-carbon dione. What could be the IUPAC NAME of this ketone? A. Butanone B. Pentanedione C Hexanone D. Butanedione 7Explain addition of H2O to an alkyne ?