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If the reaction is overheated for too long, a different with the empirical formula CsHs04 is...
How do you calculate the empirical and molecular formula of this unknown compound ? How do...
How do you calculate the empirical and molecular formula of
this unknown compound ? How do you calculate the molecular weight
?
Computer Unknown # 8 Physical Properties ВP Colorless Liquid Sweet odor C 77.75 % H-7.46 % 200-204 °C Sodium Fusion Test A portion of the sodium fusion filtrate was treated with ferrous sulfate and heated. It was then acidified with dilute sulfuric acid. No observable change was noticed. Another portion of the sodium fusion filtrate was treated with...
How do you calculate the empirical and molecular formula of this unknown compound ? How do...
How do you calculate the empirical and molecular formula of
this unknown compound ? How do you calculate the molecular weight
?
Computer Unknown # Physical Properties MP 48-51 °C White solid C = 48.27% H=3.54% Sodium Fusion Test A portion of the sodium fusion filtrate was treated and heated. It was then acidified wit was noticed. filtrate was treated with ferrous sulfate acidified with dilute sulfuric acid. No observable change Another portion of the sodium fus observable change was...
How do you calculate the empirical and molecular formula of this unknown compound ? How do you calculate the molecular...
How do you calculate the empirical and molecular formula of
this unknown compound ? How do you calculate the molecular weight
?
Computer Unknown #6 Physical Properties 210 200 BP 131-133 °C White solid Sweet odor C 79.22 % H = 5.70% 180 Sodium Fusion Tests ervable cha pordon of the sodium fusion filtrate was treated with ferrous state and heated. It was then acidified with dilute sulfuric acid. No observable ona was noticed. Another portion of the sodium fusion...
Questions and Problems 553 ation for the reaction that would produse cach of the following amines...
Questions and Problems 553 ation for the reaction that would produse cach of the following amines b. N.Methylpropanamine c. N.N-Diethylpentanamine 15.37 Briefly explain why the lower molar massamines (lewer than five carbons) exhibit appreciable solubility in water 15.38 Why is the salt of an amine appreciably more soluble in water than the mine from which it was formed 15.39 Most drugs containing amine groups are not administered as the mine but rather the amount you suggeste son why? 15.40 Why...
Working on the questions at the end of this lab report (see above). I need help answering questio...
Working on the questions at the end of this lab report
(see above). I need help answering questions 2, 3, and 4 completely
and thoroughly. Thank you!
s, until the I hexano 1 clean disti CYCLOHEXENE from CYCLOHEXANOL be dehydrated with solfuric acid to yield cyclohexene and waterf Add a 0°C (record ct and cal H,SO + H20 ainer. s in purification of any crude product are (a) the preliminary separation of the product from the reaction mixture by distillation...
VULTIPLE CHOICE points each) 1) What is TRUE about the 20mino acids used to form proteins?...
VULTIPLE CHOICE points each) 1) What is TRUE about the 20mino acids used to form proteins? a) They all are in the "L"configuration b) They are all in the form meaning the amino group is opposite the acid group e) They are all chiral. - They are all "Tertiary with four different groups attached They are all secondary with the aming group on the carbon secondary to the acid group 2) Fibrinoge is a protein involved in blood clotting. It's...
QUESTION 1 Any reaction involving a carbonyl group and a strong acid begins with the same...
QUESTION 1 Any reaction involving a carbonyl group and a strong acid begins with the same first step, which is __________________ of the carbonyl oxygen. QUESTION 2 Using condensed molecular formulas (C#H#X#Y#) for your answers, predict the products of the reactions of C6H5CH2CHO (phenylacetaldehyde) with these reagents, and identify the functional group produced in the product. Note that the Tx symbol above allows you to do a subscript. a. NaBH4 / CH3OH b. 1. CH3MgBr; 2. H2O c. Ph3P=CHCH3 d....
**(left structure)****(right structure)** The two structures for the assignment are above and the task is: 1....
**(left structure)****(right
structure)**
The two structures for the assignment are above and
the task is:
1. Perform a retrosynthetic analysis on the two target
molecules assigned to you. In each case the organic
starting material (what you have to work backwards toward) depends
upon the target. For the structure given above (structure on left),
the starting material is either malonic ester or acetoacetic ester
and any halide. For the structure given above (structure on right),
the starting material is any...
Group I Cations A INTRODUCTION Most metal halides are soluble in water and dilute hydrochloric acid....
Group I Cations A INTRODUCTION Most metal halides are soluble in water and dilute hydrochloric acid. The exceptions are silver ion, Ag mercurous ion, Hg,: and lead(II) ion, Pb. Consequently, the addition of HCI to a solution of metal cations leads to the selective precipitation of these three ions. While the theory behind the separation and identification of these ions has been outlined in the general discus- sion of the qualitative analysis scheme, some aspects of this chemistry need to...
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules...
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the organic starting material (what you have to work backwards toward) depends...
How do you calculate the empirical and molecular formula of
this unknown compound ? How do you calculate the molecular weight
?
Computer Unknown # 8 Physical Properties ВP Colorless Liquid Sweet odor C 77.75 % H-7.46 % 200-204 °C Sodium Fusion Test A portion of the sodium fusion filtrate was treated with ferrous sulfate and heated. It was then acidified with dilute sulfuric acid. No observable change was noticed. Another portion of the sodium fusion filtrate was treated with...
How do you calculate the empirical and molecular formula of
this unknown compound ? How do you calculate the molecular weight
?
Computer Unknown # Physical Properties MP 48-51 °C White solid C = 48.27% H=3.54% Sodium Fusion Test A portion of the sodium fusion filtrate was treated and heated. It was then acidified wit was noticed. filtrate was treated with ferrous sulfate acidified with dilute sulfuric acid. No observable change Another portion of the sodium fus observable change was...
How do you calculate the empirical and molecular formula of
this unknown compound ? How do you calculate the molecular weight
?
Computer Unknown #6 Physical Properties 210 200 BP 131-133 °C White solid Sweet odor C 79.22 % H = 5.70% 180 Sodium Fusion Tests ervable cha pordon of the sodium fusion filtrate was treated with ferrous state and heated. It was then acidified with dilute sulfuric acid. No observable ona was noticed. Another portion of the sodium fusion...
Questions and Problems 553 ation for the reaction that would produse cach of the following amines b. N.Methylpropanamine c. N.N-Diethylpentanamine 15.37 Briefly explain why the lower molar massamines (lewer than five carbons) exhibit appreciable solubility in water 15.38 Why is the salt of an amine appreciably more soluble in water than the mine from which it was formed 15.39 Most drugs containing amine groups are not administered as the mine but rather the amount you suggeste son why? 15.40 Why...
Working on the questions at the end of this lab report
(see above). I need help answering questions 2, 3, and 4 completely
and thoroughly. Thank you!
s, until the I hexano 1 clean disti CYCLOHEXENE from CYCLOHEXANOL be dehydrated with solfuric acid to yield cyclohexene and waterf Add a 0°C (record ct and cal H,SO + H20 ainer. s in purification of any crude product are (a) the preliminary separation of the product from the reaction mixture by distillation...
VULTIPLE CHOICE points each) 1) What is TRUE about the 20mino acids used to form proteins? a) They all are in the "L"configuration b) They are all in the form meaning the amino group is opposite the acid group e) They are all chiral. - They are all "Tertiary with four different groups attached They are all secondary with the aming group on the carbon secondary to the acid group 2) Fibrinoge is a protein involved in blood clotting. It's...
**(left structure)****(right
structure)**
The two structures for the assignment are above and
the task is:
1. Perform a retrosynthetic analysis on the two target
molecules assigned to you. In each case the organic
starting material (what you have to work backwards toward) depends
upon the target. For the structure given above (structure on left),
the starting material is either malonic ester or acetoacetic ester
and any halide. For the structure given above (structure on right),
the starting material is any...
Group I Cations A INTRODUCTION Most metal halides are soluble in water and dilute hydrochloric acid. The exceptions are silver ion, Ag mercurous ion, Hg,: and lead(II) ion, Pb. Consequently, the addition of HCI to a solution of metal cations leads to the selective precipitation of these three ions. While the theory behind the separation and identification of these ions has been outlined in the general discus- sion of the qualitative analysis scheme, some aspects of this chemistry need to...
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the organic starting material (what you have to work backwards toward) depends...
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