Nitrosyl chloride, NOCl, can be used as a nonaqueous solvent. It can undergo autodissociation with NO+...
Nitrosyl chloride, NOCl, can be used as a nonaqueous solvent. It can undergo autodissociation with NO+ and Cl– as the products. Identify which of the ions is a Lewis acid and which is a Lewis base, and explain why.
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Nitrosyl chloride, NOCl, can be used as a nonaqueous solvent. It
can undergo autodissociation with NO+...
Draw three resonance structures for nitrosyl chloride (NOCl) and assign formal charges to each atom. (Nitrogen...
Draw three resonance structures for nitrosyl chloride (NOCl) and assign formal charges to each atom. (Nitrogen is the central atom) A) Which resonance structure is favored by formal charge considerations & why? B) For the favored resonance structure, what is the electron and molecular geometry around the nitrogen atom? What is the bond angle?
there is no more info to add Consider the following equilibrium: ci2) and 2.39 atm of nitrosyl chloride NOCl at 595·℃ Answer the following questions Now suppose a reaction vessel is filled with 9.28...
there is no more info to add
Consider the following equilibrium: ci2) and 2.39 atm of nitrosyl chloride NOCl at 595·℃ Answer the following questions Now suppose a reaction vessel is filled with 9.28 atm of chlorine about this system: O rise Under these conditions, will the pressure of NOCl tend to rise or fall? O fall ク is it possible to reverse this tendency by adding NO? In other words, if you said the pressure of NoCl will tend...
. Can methanol be used as a solvent in the deprotonation of a terminal alkyne by...
. Can methanol be used as a solvent in the deprotonation of a terminal alkyne by sodium amide, NaNH,? Explain. You will need to set up two acid base equillibria to answer this question properly.
Arsenic trichloride can act both as a Lewis acid and as a Lewis base. Explain why...
Arsenic trichloride can act both as a Lewis acid and as a Lewis base. Explain why this is so and write a balanced equation for each using BF3 and Cl− as reaction partners. 1,Write the balanced equation with AsCl3 acting as Lewis base. 2,Write the balanced equation with AsCl3 acting as Lewis acid.
How can I tell which substances are donating electrons and which are accepting electrons? Identify the...
How can I tell which substances are donating electrons and
which are accepting electrons?
Identify the Lewis acid and Lewis base that lead to the formation of the following species: (a) AICI, (b) Cd(CN) (c) HCO3, (d) H SO (a) AlCl3 + Cl → AICIG AIC13 (Lewis acid), CI (Lewis base) Cd²+ (Lewis acid), CN (Lewis base) (b) Cd2+ +4CN Cd(CN) (c) H+ + což – HCO3 (d) H+ + HS04 — H2SO4 H (Lewis acid), COŽ- (Lewis base) H...
Explain in a few sentences how extraction can be used to separate an organic compound from sodium chloride.
06 Lab 3a Separation.pdfQuestion 1 of prelabExplain in a few sentences how extraction can be used to separate an organic compound from sodium chloride.
Prelab
1. Explain in a few sentences how extraction can be used to separate an organic compound from
sodium chloride.
2. Why is the CH2Cl2 layer the bottom layer in a CH2Cl2 / aqueous NaHCO3 extraction? In this
experiment, what does the CH2Cl2 layer contain? What does the aqueous NaHCO3 layer
contain?
3. In general, how...
Diethyl ether is a good solvent to be used with Grignard reagents. Which of the following...
Diethyl ether is a good solvent to be used with Grignard reagents. Which of the following explanations for this laat alle! It can serve as a Lewis base and stabilize the Grignard reagent. It has a very high boiling so it can be heated to drive the Grignard formation to completion. It is polar enough to stabilize the Grignard reagent. It is aprotic and thus is not acidic enough to react with the Grignard reagent.
Carboxylic acid esters can undergo acid catalyzed hydrolysis, neutral hydrolysis and base catalyzed hydrolysis. Below is...
Carboxylic acid esters can undergo acid catalyzed hydrolysis, neutral hydrolysis and base catalyzed hydrolysis. Below is a table with three structurally related carboxylic acid esters and the second order reaction rate constants for the acid-catalyzed mechanism (k_A) and the rate constant for the base-catalyzed mechanism (k_B). The difference between the three compounds is mainly the substitution of hydrogen atoms on R_1 with the more electronegative chlorine atoms. a) Explain why there is only a small change in k_A for the...
please help! a)asses substrate b) classify reagents (nuc/base, strong or weak) c)solvent used if not indicated...
please help! a)asses substrate b) classify reagents (nuc/base, strong or weak) c)solvent used if not indicated d)mechanism type e)major & minor products including stereochemistry & geometry nuc inuetral + cl NaCI DMF weak ba 14. conc. H2SO4 A 20
12. Which is the major product of the reaction shown? (a) (b) (c) (d) 13. What...
12. Which is the major product of the reaction shown? (a) (b)
(c) (d) 13. What are all of the possible products formed in the
following reaction? (choose all correct answers) (a) (b) (c) (d)
(e) (f) 14. The three compounds below can form a carbocation in the
presence of H2O and H2SO4. Which ones will form the same
carbocation? (a) I and II (b) I and III (c) II and III (d) all
three will form the same carbocation...
there is no more info to add
Consider the following equilibrium: ci2) and 2.39 atm of nitrosyl chloride NOCl at 595·℃ Answer the following questions Now suppose a reaction vessel is filled with 9.28 atm of chlorine about this system: O rise Under these conditions, will the pressure of NOCl tend to rise or fall? O fall ク is it possible to reverse this tendency by adding NO? In other words, if you said the pressure of NoCl will tend...
. Can methanol be used as a solvent in the deprotonation of a terminal alkyne by sodium amide, NaNH,? Explain. You will need to set up two acid base equillibria to answer this question properly.
How can I tell which substances are donating electrons and
which are accepting electrons?
Identify the Lewis acid and Lewis base that lead to the formation of the following species: (a) AICI, (b) Cd(CN) (c) HCO3, (d) H SO (a) AlCl3 + Cl → AICIG AIC13 (Lewis acid), CI (Lewis base) Cd²+ (Lewis acid), CN (Lewis base) (b) Cd2+ +4CN Cd(CN) (c) H+ + což – HCO3 (d) H+ + HS04 — H2SO4 H (Lewis acid), COŽ- (Lewis base) H...
Diethyl ether is a good solvent to be used with Grignard reagents. Which of the following explanations for this laat alle! It can serve as a Lewis base and stabilize the Grignard reagent. It has a very high boiling so it can be heated to drive the Grignard formation to completion. It is polar enough to stabilize the Grignard reagent. It is aprotic and thus is not acidic enough to react with the Grignard reagent.
Carboxylic acid esters can undergo acid catalyzed hydrolysis, neutral hydrolysis and base catalyzed hydrolysis. Below is a table with three structurally related carboxylic acid esters and the second order reaction rate constants for the acid-catalyzed mechanism (k_A) and the rate constant for the base-catalyzed mechanism (k_B). The difference between the three compounds is mainly the substitution of hydrogen atoms on R_1 with the more electronegative chlorine atoms. a) Explain why there is only a small change in k_A for the...
please help! a)asses substrate b) classify reagents (nuc/base, strong or weak) c)solvent used if not indicated d)mechanism type e)major & minor products including stereochemistry & geometry nuc inuetral + cl NaCI DMF weak ba 14. conc. H2SO4 A 20
12. Which is the major product of the reaction shown? (a) (b)
(c) (d) 13. What are all of the possible products formed in the
following reaction? (choose all correct answers) (a) (b) (c) (d)
(e) (f) 14. The three compounds below can form a carbocation in the
presence of H2O and H2SO4. Which ones will form the same
carbocation? (a) I and II (b) I and III (c) II and III (d) all
three will form the same carbocation...
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