1) In the reaction between keone ( benzophenone ) and excess alcohol ( 2 equivalent ) in presence of acid catalyst produces an ketal compound .
The detail reaction mechanism for the ketal formation is shown below .
2 ) Option C is the correct
answer .
The detail reaction mechanism for the product formation is shown below .
Predict the product © Excess CH₃CH₂OH H₂Soci Predict the product when 4-methyl-2-hexanone reacts with methylamine in...
please help me in all sections asap!!
Predict the product of the following reaction sequence. NaCN 1. LiAIHA HCN 2. H2O H2N NH2 но NH2 но но CN H2N H2N IV We were unable to transcribe this imagePredict the product for the following reaction. ОН excess 1. NH2NH2/H 2. KOH/ H2O/A NNH2 CH H_NHNH2 NH OH 0 CH CH NNH OH HO NHNH 0 NH IV v Predict the product of the following reaction sequence. NaCN HCN NH2 H2N но...
please help in all sections asap!!
Predict the product of the following reaction. CH3COOH ОН ОН Compound A on ozonolysis yields the following two products What is the structure of compound A? Compound A 1.03 2. (CH3)25 OV none of these Predict the product(s) for the following reaction. H30 OH We were unable to transcribe this imageA compound with an OH and an OR group attached to the same carbon is known as an acetal a hemiacetal a hydrate a...
40. (38) Predict the product or provide reagents needed to complete each transformation. OH (a-b) K+-OH excess OH OF 1. SOCI Na+ HCO3- (c-d) 2. NH3 OH 1. KOH 2. CH CH CH Br ol (e-t) NH 3. NHANH H, H2, Pd ?? ?? (g-h) 'Ng NH2 NO2 (g-k) NEN OH 1. CH3 2. Ag20 3. heat 1. CH 2. Ag2O 3. heat (I-m) NH2 OH ?? NEN ?? (n-O) CI CI CI 1. Mg, ether 2. CO2 CH3CH2NH2, H+...
40. (38) Predict the product or provide reagents needed to complete each transformation. OH A (a-b) K-OH excess OH Na+ HCO3-. (c-d) 1. SOCI 2. NH, OH 1. KOH 2. CH3CH2CH Br a H (e-f) NH 3. NHỊNH H, Hz. Pd ?? ?? (g-h) N3 NH2 NOZ (g-k) -NEN OH CI N 1. CH3 2. Ag20 3. heat 1. CHE 2. Ag20 3. heat (l-m) NH2 ?? NEN OH ?? (n-0) CI CI CI CI (put) 1. Mg, ether 2.Co,...
dehydes and ketones [References) Draw the product that would result when 3-hexanone reacts with an excess of l-propanol in the presence of an acid catalyst - OVO - IF
Question 20 Predict the product for the following reaction sequence. OH Na Cr2O7/H2SO4/H2O SOCI excess NH3 SOCI 1. CH3CH2MgBr 2. H307 HO NH2 - 0 NH2 1 Chapter 10 Notes Spot Chapter20_Notes (13pdf Search
Provide the major product or reagents
OH (a-b) K-OH excess OH NaHCO, (c-d) 1. SOCI 2. NH OH e-t) NH 1. кон 2. CH CH CH.BI 3. NHANH H. Hy Pd 22 ?? (g-h) NH NO (g-k) OH 1. CH 2. Ag,0 3. heat 1. CH 2. Ag, 3. heat (l-m) NH OH ?? ?? (n-o) CI (p-1) 1. Mg, other 2.CO 3.H.,0,H CH,CHÁNH, H+ Δ ?? 1" O 1. LAIH4 CH,CH,OH, H осн. A 2. H,O, H.
please help in all sections asap!!!!
Which of the following reagent(s) could not be used to carry out the following transformation? HSCH2CH2SH, BFy; then Raney NI (H) 1. NH NH/H"; 2. KOH/H20/heat LAH, ether Zn(Hg), HCI Predict the product for the following reaction. О, Н excess 1. NH2NH2/H 2. KOH/ H2O/A NNH2 HO. Η ΝΗΝΗΣ NH2 CH OH CH CH HOCHNHNH OH NH2 NNH2 IN V We were unable to transcribe this imagePredict the product(s) for the following reaction. NaOH...
Lumili alle for the following compound? - (CH)CHCH.COCH,CH, a. 2-methyl-4-hexanone c. 2-methyl-3-hexanone b. 5-methyl-3-hexanone d. ethyl isopropyl ketonel. 25-Identify the directing effect of the ring substituent in the following reaction: BO, HBO. (a) o.p., activating (b) m-, deactivating (c) o.p., deactivating (d) None of these 26--Ketones are easily reduced to CH3-C-CH3 a-Secondary alcohol b- Primary alcohol c- to acetaldehyde d- to carboxylic acid 27-. What is the structure of the azo group? a-N- b-N-N- C-NEN- d-NEN- 28-What class of organic...
14. (4 points each) Complete the following reactions showing the major organic product). 2 CH,NH CH CH,OH Ci pyridine 2. 2CH,NH2 Ci AICl I. excess CH,MgBr 2. H CH,CH,CH OH NaOH
14. (4 points each) Complete the following reactions showing the major organic product). 2 CH,NH CH CH,OH Ci pyridine 2. 2CH,NH2 Ci AICl I. excess CH,MgBr 2. H CH,CH,CH OH NaOH