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5. Amides and esters. Fill in the necessary reagents (at least, half of them). de dae...
Fill in the sentences: WORD BANK: Amino Acids, Amides, Phosphates, Monosaccharides, Esters, Ethers, Ketones, Aldeyhyde Proteins...
Fill in the sentences: WORD BANK: Amino Acids, Amides, Phosphates, Monosaccharides, Esters, Ethers, Ketones, Aldeyhyde Proteins are composed of BLANK, linked by BLANK. Nucleotides contain up to three BLANK. Polysaccharides are composed of monosaccharides linked by BLANK
Question 4 Waxes are high molar mass: A)Fatty acids B) Esters C)Alcohols D) Amides B Question...
Question 4 Waxes are high molar mass: A)Fatty acids B) Esters C)Alcohols D) Amides B Question 5 Provide the reagent(s) necessary to carry out the following conversion. COCHE OH A) 1) one equivalent CH3MgBr/ether 2) H2O B) excess CH3MgBr/ether/H2O C) 1) excess CH3MgBr/ether 2) H2O D) all the above A В C Question 6 Which one is not a complex lipid? AyWaxes B) steroids Phospholipids D) Triglycerides A B С D
Fill in necessary reagents -------------------->>>>>>> I have an idea to radical brominate and then generate...
Fill in necessary reagents
-------------------->>>>>>>
I have an idea to radical brominate and then generate grignard
and then react with trimethyl amine but I dont think thats right...
Or else brominate, then chain extension, then substitution somehow
but i dont think thats right either... Or something to do with
cyanide ion? Im stuck it's the only one i cant figure out and i
cant find in the book and its due tomorrow.
I have an idea to radical brominate...
Fill in the following rxn webs by adding the necessary reagents to complete the indicated transformations...
Fill in the following rxn webs by adding the necessary reagents
to complete the indicated transformations
Br Br Br man - ܝܗ ܀ -CH3 H Br Br Br Br Br OH Br
Map de Show any steps, reagents and conditions necessary to efficiently carry out the following muti-step...
Map de Show any steps, reagents and conditions necessary to efficiently carry out the following muti-step transformations from the starting material on the left to the product on the right. Do not worry about stereochemistry.
10. Part A. (9 pt) Fill in any necessary reagents or intermediates in the empty boxes...
10. Part A. (9 pt) Fill in any necessary reagents or intermediates in the empty boxes in the scheme below. 2) DMS 1) LAH 52) H30+ / H20 PCC/ CH2Cl2 W + En сон 1) OsO4 2) NaHSO3 /H20 + 3 other stereoisomers.
13. (15) For each a For each of the following reactions, fill in the missing reagents...
13. (15) For each a For each of the following reactions, fill in the missing reagents from the list provided for Wormation of the product shown. Sequential steps, if necessary. should be numbered. Reagents can be used more than once. Reagent List: H2 C H2O2 = NaH PBT OCI NaBH. Pd/C NaOH BH2O HO HgCl2 Pd/Caco, Br2 HBr H2O (HOAC) (MCPBA) (pyridine) (Msch) por -Cl menos de plaqueta don -он i н он
please write clear ☺️ thank u!!! to fill in thr reagents necessary to get thosr products...
please write clear ☺️ thank u!!!
to
fill in thr reagents necessary to get thosr products shown from
each starting product.
wy "N(CH2 box C ОН box A box B Chemical Formula Cha HO Chemical Formula CHIO box D CH,0
4. Do All parts: a. Provide the reagents necessary to carry out the following conversion (5...
4. Do All parts: a. Provide the reagents necessary to carry out the following conversion (5 points) b. Provide the reagents necessary to carry out the following conversion. (5 points)
Identify the reagents necessary to achieve each of the transformations below. HINT: You will need to...
Identify the reagents necessary to achieve each of the
transformations below.
HINT: You will need to use at least one reaction from this chapter
and at least one reaction from the previous chapter. The essence of
this problem is to choose reagents that will achieve the desired
stereochemical outcome:
Choose from reagents (A-H): 1) Na, NH3 ( 1) H2, Lindlar's catalyst 2) OsO4, NMO 2) Br2 1) Na, NH3 () 1) NaNH2 4) Mel 2) Mel 5) Na, NH3 ()...
Question 4 Waxes are high molar mass: A)Fatty acids B) Esters C)Alcohols D) Amides B Question 5 Provide the reagent(s) necessary to carry out the following conversion. COCHE OH A) 1) one equivalent CH3MgBr/ether 2) H2O B) excess CH3MgBr/ether/H2O C) 1) excess CH3MgBr/ether 2) H2O D) all the above A В C Question 6 Which one is not a complex lipid? AyWaxes B) steroids Phospholipids D) Triglycerides A B С D
Fill in necessary reagents
-------------------->>>>>>>
I have an idea to radical brominate and then generate grignard
and then react with trimethyl amine but I dont think thats right...
Or else brominate, then chain extension, then substitution somehow
but i dont think thats right either... Or something to do with
cyanide ion? Im stuck it's the only one i cant figure out and i
cant find in the book and its due tomorrow.
I have an idea to radical brominate...
Fill in the following rxn webs by adding the necessary reagents
to complete the indicated transformations
Br Br Br man - ܝܗ ܀ -CH3 H Br Br Br Br Br OH Br
Map de Show any steps, reagents and conditions necessary to efficiently carry out the following muti-step transformations from the starting material on the left to the product on the right. Do not worry about stereochemistry.
10. Part A. (9 pt) Fill in any necessary reagents or intermediates in the empty boxes in the scheme below. 2) DMS 1) LAH 52) H30+ / H20 PCC/ CH2Cl2 W + En сон 1) OsO4 2) NaHSO3 /H20 + 3 other stereoisomers.
13. (15) For each a For each of the following reactions, fill in the missing reagents from the list provided for Wormation of the product shown. Sequential steps, if necessary. should be numbered. Reagents can be used more than once. Reagent List: H2 C H2O2 = NaH PBT OCI NaBH. Pd/C NaOH BH2O HO HgCl2 Pd/Caco, Br2 HBr H2O (HOAC) (MCPBA) (pyridine) (Msch) por -Cl menos de plaqueta don -он i н он
please write clear ☺️ thank u!!!
to
fill in thr reagents necessary to get thosr products shown from
each starting product.
wy "N(CH2 box C ОН box A box B Chemical Formula Cha HO Chemical Formula CHIO box D CH,0
4. Do All parts: a. Provide the reagents necessary to carry out the following conversion (5 points) b. Provide the reagents necessary to carry out the following conversion. (5 points)
Identify the reagents necessary to achieve each of the
transformations below.
HINT: You will need to use at least one reaction from this chapter
and at least one reaction from the previous chapter. The essence of
this problem is to choose reagents that will achieve the desired
stereochemical outcome:
Choose from reagents (A-H): 1) Na, NH3 ( 1) H2, Lindlar's catalyst 2) OsO4, NMO 2) Br2 1) Na, NH3 () 1) NaNH2 4) Mel 2) Mel 5) Na, NH3 ()...
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