(a)
Interpretation: The products that are formed by the reaction of the given terminal
Concept introduction: A stepwise procedure of transforming an alkyne into a carbonyl group is known hydroboration-oxidation reaction. In a hydroboration-oxidation reaction, a terminal alkyne reacts with
A terminal alkyne reacts with
(b)
Interpretation: The products that are formed by the reaction of the given terminal alkyne, with [1]
Concept introduction: A stepwise procedure of transforming an alkyne into a carbonyl group is known hydroboration-oxidation reaction. In a hydroboration-oxidation reaction, a terminal alkyne reacts with
A terminal alkyne reacts with
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- Bromo cyclopentadiene reacts to form a Witting Reagent (A), but does not react with aldehydes or ketones to give an alkene. Draw A and explain why it does not react with a carbonyl. Br 1. PPh3 2. Base A R H No Rxarrow_forwardWhat ester is formed when each carboxylic acid is treated with ethanol (CH 3CH 2OH) in the presence of H 2SO 4?arrow_forwardDraw the major product of the reaction between 1-butanol and Na2Cr207, H2SO4, H2O. O, O, e CHarrow_forward
- When alkyne A is treated with NaNH2 followed by CH3I, a product having molecular formula C6H10O is formed, but it is not compound B. What is the structure of the product and why is it formed?arrow_forward5. Give the IUPAC name of the following carboxylic compounds. а. СН,CH,С3ССООН b. CH;CH(NH;)CH(OH)COOH c. (CH;)C=CHCOOH d. CH3 СООН е. NO, COOH O,N 'NO2arrow_forwardQ#7 Draw the organic products formed in each reaction. Br -OC(CH3)3 -OCH,CH3 b. CI CI NH2 (2 equiv) Br DBU d. -Oc(CH3)3 Br Br CH3CH2OH f. 1. a. C. e.arrow_forward
- Q10arrow_forwardDraw the products formed when phenol (C6H5OH) is treated with each set of reagents. a. [1] HNO3, H2SO4; [2] Sn, HCl b. [1] (CH3CH2)2CHCOCl, AlCl3; [2] Zn(Hg), HCl c. [1] CH3CH2Cl, AlCl3; [2] Br2, hν d. [1] (CH3)2CHCl, AlCl3; [2] KMnO4arrow_forwardWhich ester can be easily condensed with sodium ethoxide to produce B-keto ester? Ph-C-OEt CH3-CH, C-OEt В. CH,-CH-C-OEt С. CH, 0 ҫ Н D. °f" A. 8 ČH, Öarrow_forward
- The following product can be synthesized from the reaction of an alkene with Hg(OAc)2 followed by reduction with NaBH4. Draw all possible alkenes that will give the product shown.arrow_forwardDraw the organic products formed in each reaction.arrow_forwardDraw the product formed when pentanal (CH;CH,CH2CH;CHO) is treated with each reagent. With some reagents, no reaction occurs. a. NaBH4, CH,OH b. [1] LIAIH4; (2] H20 c. H2, Pd-C d. PCC e. NazCr,07, H2SO4, H2O f. Ag,0, NH,OH g. [1) CH,MgBr; (2] H2O h. [1] CęH,Li; [2] H20 i. [1] (CH3),CuLi; (2] H2O j. [1] HC=CNa; [2] H2O k. [1] CH;C=CLi; [2] H2O I. The product in (a), then TBDMS-CI, imidazolearrow_forward