Converting aldehydes to primary alcohols is Reduction process.
-CHO is changes to -CH2OH group.
Out of the given reagents KMnO4 is oxidising agent.
Br2/CCl4 is also oxidising agen (by brominatinng unsaturation)
H2/ Ni is a strong reducing agent which reduces aldehydes to promary alcohols , ketones to secondary alcohols and unsaturation compound to saturation comppunds.
( Sodium Borohydride) is also reducing agent but it cannot reduce unsatiration .
Sodium borohydride is mild reducing agent and it is not strong like LiAlH4 ( Lithium aluminuum Hydride.)
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So of the given the are two options H2/Ni and NaBH4
But H2/Ni is capable enough to reduce completely given 3-Heptanal to n-Heptanol
So best choice is H2/Ni
Which of the reagents listed below would efficiently accomplish the transformation of CH,CH,CH=CHCH,CH,CHO into CHỊCH,CH,CH,CH,CH,CH,OH? 4...
Which of the reagents listed below would efficiently accomplish the transformation of CHỊCH CH=CHCHÚCH CHO into CH3CH2CH2CH2CH2CH2CH2OH? Select one or more: O a. KMnO Ob. NaBHA Oc. Br, in CCIA Od. H2, Ni Oe. Two of these choices.
6. Which of the reagents listed below would efficiently accomplish the transformation of CH3CH2CH=CHCH2CH2CHO into CH3CH2CH=CHCH2CH2CH2OH? a) KMnO4 b) NaBH4 c) Br2 in CCl d) H2, Ni e) Two of these choices. I
CH,CH,CHCHCCH, CHỊCH,CH,CH-OH CHỊCH,CH,CH,CHCH CH,CH,CHOH 1. Using IR spectroscopy describe how you would distinguish between each pair of compounds. i CH,CH.CCH CH,CH.COCH and 2. How would you use IR spectroscopy to decide if the reaction below had occurred? CH CH Base Heat 3. Match the IR spectra below to one of the four compounds above them.
4. (3 pt) Which synthesis below would work best for the following transformation? OH A. 1. Mg in ether, 2. CH CHO with an H+ workup B. 1. MeLi, 2. CH CHO with an H+ workup C. NaOMe and heat D. NaBH, then H+ workup
Propose a synthesis of the following derivative of diethyl malonate using reagents from the choices provided below. (From the choices provided, list the reagent(s) in order that will accomplish this transformation. No more than 4 steps are required. List your answer as a single letter (single-step transformation) or a series of letters (multi-step transformation) with no commas separating them.) Reagents available a. Eto Na g. CH2=CHCH=CHCH,Br b. CH3 CH2Br c. CH3 CH, CH, CH(CH3)Br d. (CH3)2 CHCH, CH,Br e. CH3...
Choose reagents from the table to accomplish transformations in the scheme below. List reagents by letter CO,Et 3 5 7 (a reduction) COGER 4 Reagents a Naot / ETOH Hy over Pd/C Hy0*/H2O room temp H,Oheat b Trace of HShea NaOet then BACH,COEU KMnO/H30 g NaOet, then CH,B! k LIAIH, then H,09 d NaBH then H30 h CH,CH,OH/HCI - POC pyridine Steps Step 6 Step7 Step
Which reagent or set of reagents will best accomplish this transformation? b OH (A) OsO (B) 1) Hg(OAc); /H:0 2) NaBH, I-BOOH (D) HOOH (C) 1) THF-BH, 2) H-02/OH/H,0 7 What is the product of this reaction? (A) W model Å Which best represents a step in the mechanism for " I- @ AR .-
Which set of reagents will accomplish the following transformation? COOH NH Br A) B) C) 1) CH;CI / AICI 2) Br2/FeBrz 3) Conc. KMnO4 OH, A. then H30 4) Cl2/AICI; 5) HNO3 H2SO4 6) Sn/HCI 1) CH3C1 / AICI 2) Conc KMnO4 OH, A, then H30* 3) HNO; / H2SO4 4) Sn HCI 5) Bry/FeBrz 6) C12/AICI: 1) CH,CI/AICI: 2) Bry/FeBrz 3) Cly/AICI: 4) Conc. KMnO OH, Athen H30 5) HNO3 /H SO. 6) Sn/HCI B) D) 1) HNO; H2SO4...
answer all 3 questions pls In which region of the 13C NMR spectrum do you expect the resonance of the following carbon to appear? OH Select one: a. 140-220 ppm b. 110-140 ppm Oo oo C. 50-80 ppm d. 75-100 ppm Which of the following reagents is the best choice to carry out the transformation shown here? Select one: o a. Croz, H,0 2 b. C,HNCO,C1, CH,C, O C. Na, Cr,,,H,O, HOẶC 0 d. NaOCI, HOẶC What is the major...
References From the lists of available reagents select the one(s) you would use to in a preparation of acetophenone (phenyl methyl katone) from methylberate (In no case are more than three steps necessary.) . SOCH Reagents Available a CH,COCI, AICI d. CH CHO g. Mg b. (CH3)2Culi e. Ho(OA), H,Othen NaBH, h. NaOH, H, C. CH, MgBr, then H30* . KMnO, H2O 1. Dess-Martin periodinane List reagents by letter in the order that they are used; example: la Reagents used:...