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option d vs e 15) What compound is produced when N,N-dimethylpropanamide is treated with LiAlH4? A)...
Please answer all questions 13) Which of the following are intermediates in the acid hydrolysis of an amide? Hyo. he at NH, SOH но он HO, OH RANH NH RAH он RNH н н 2 4 A) 1 B) 2 C) 2 & 3 D) 4 E) 1, 2, & 3 14) Acids can be reduced to aldehydes by A) treatment with LiAlH4 B) conversion to the acid chloride followed by treatment with LiAlH[OC(CH3)313 C) conversion to the amide followed...
Compound A, C11H12O, which gave a negative Tollens test, was treated with LiAlH4, followed by dilute acid, to give compound B, which could be resolved into enantiomers. When optically active B was treated with CrO3 in pyridine, an optically inactive sample of A was obtained. Heating A with hydrazine in base gave hydrocarbon C, which, when heated with alkaline KMnO4, gave carboxylic acid D. Identify compounds A, B, and C.
please help & please explain! . Which compound would be formed when 2-methylbutanal is treated with a solution of NaOD in D O? A) CH3CHDCHCHO B) CH2DCH CHCHO C) CH3CH2CHCDO D) CH3CH2CDCDO E) CH3CH2CDCHO CH3 CH3 CH3 CH3 CH3
all part of a big question please answer all neatly. What is the major product in the following reaction? CH,CH-Mgelether Page 1 4 3. H,O/heat D Cyclic esters are called: A) lactones. B) lactams C) lacrimals D) imides What compound is produced when N,N-dimethylacetamide (shown below) is treated with LIAIH4? A) CH3CH2CON B) CH3CH2CH2NH су сHаCHзCH2Oн D) CH3CH2CH2N(CH32 E) CH3CH2N(CH3)2 X A AA What is the major product in the following reaction? Page | 5 Pyridine HyC What are the...
What product is obtained when y-lactam is treated with LiAlH4 followed by water? 1. LiAIH, =0 2. H၇ဝ y-lactam image A. -OH image O B. image HOOC `NH၇ image NH2 HO
7. When compound 1 is treated with concentrated HBr, it yields the corresponding compound 2. Propose a mechanism that will account for the stereochemistry of the reaction. Br CH3 Br CH3 H Hl.... C + HBr C6-H HI CHE OH CH3
When the following optically pure compound (1) is treated with NaN3 in THF (tetrahydrofuran = the solvent) followed by an acidic work-up it is found that for step #1, the rate of formation of the product is tripled when the concentration of NaN3 is tripled. Which is the expected major product? 6. The reaction in question #5 proceeded via which mechanism? a. E1 b. E2 c. SN1 d. SN2 e. SN2´ (allylic displacement) 5. When the following optically pure compound...
What is the product when the compound below is treated with aqueous acid? Identify the expected products when the following compound is treated with aqueous acid. нас нас н HC - CH₂ B) H₃C, 0 46. ict C) HyC CH₂ H₃ CH₃ エーz D H3C C HE _CH₂ H₃ CH₃
2. t-butoxide/t-butanol E) 1. TsCl/pyridine 2. LiAIH4 19) What compound results when 1-butanol is treated with P/l2? A) CH3CH2CH2CH2I B) racemic CH3CH2CHICH3 C) CH3CH2CH2CH20P(OH)2 D) CH3CH2CH2CH2Pl2 E) Primary alcohols don't react with P/12 7
What are all of the products when this compound is treated with NBS and irradiated with UV light? treated with NBS with UV light, five dif- e Ot enan roduct that is obtainec