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For the following reaction, which reaction will be faster (Left or Right)? Why? Click on the...
Draw the major product of this reaction only. OTS acetone CH3 For the following reaction, which reaction will be fa...
Draw the major product of this reaction only. OTS acetone CH3 For the following reaction, which reaction will be faster (Left or Right)? Why? Click on the reaction that will be faster AND the right reason V1 + OH - or 1 + OOCCH3 Left Right Because the correct answer performs an elimination reaction while the incorrect one does a substitution reaction Because the correct answer has a stronger base than the incorrect answer. Resonance makes a stronger base. Because...
For the following reaction, which reaction will be faster (Left or Right)? Why? Click on the reaction that will be...
For the following reaction, which reaction will be faster (Left or Right)? Why? Click on the reaction that will be faster AND the right reason Br +CH OH — ory Br + CH, OH Left Right Because the correct reaction is SN1 and the incorrect reaction is E1. Substitution reactions are more stable than elimination reactions Because the correct reaction doesn't have a double bond. Double bonds make unstable carbocations Because the correct reaction has resonance. The resonance structures allow...
7. Which statement is true about the acid/base equilibrium reaction? ASH OH (A) The right side...
7. Which statement is true about the acid/base equilibrium reaction? ASH OH (A) The right side is favored because the base on the right side is the stronger of the two bases. (B) The right side is favored because the base on the right side is more stable. (C) The left side is favored because the base on the left side is weaker. (D) The right side is favored because we always draw reactions such that the right side is...
please answer all questions The major product of this reaction is (4) CF NH. (B) CF...
please answer all questions
The major product of this reaction is (4) CF NH. (B) CF (C) CF (D) no reaction CH, CH=24CH, beat The product of this rearrangement is (c) H 14 CH CHCH. (D) CH-CH2CH2 0.« *0. Which is not a reason this reaction fails to take place? (A) The C to which Cl is bonded is sp hybridized, making a shorter and stronger bond than those usually broken in substitution reactions. (B) Resonance gives the bond between...
When determining which mechanism (E1 or E2) occurs, the following process is helpful: 1) Determine the...
When determining which mechanism (E1 or E2) occurs, the following process is helpful: 1) Determine the substitution (methyl, 1º, 2º, or 3“) of the alkyl halide 2) Determine the strength of the nucleophile Please fill out the following table, indicating the category of reaction (E1 or E2) that will occur in each set of alkyl halides and nucleophiles. If no reaction occurs, write 'NR: Alkyl Halide Strong Base Weak Base Methyl 1° 20 3° For each of the following reactions,...
If the acid-base reaction NH2- + HSO4- ⟺ NH3 + SO42- proceeds to the right as...
If the acid-base reaction NH2- + HSO4- ⟺ NH3 + SO42- proceeds to the right as written, then we must conclude that Group of answer choices NH2- is a stronger base than SO42-. NH3 is a stronger acid than HSO4-. NH3 is a stronger base than NH2-. NH3 is a weaker acid than NH2-. NH3 is a weaker base than HSO4-.
Does the equilibrium lie to the left or the right? Explain why (what makes the acid...
Does the equilibrium lie to the left or the right? Explain why (what makes the acid or base weaker or stronger) sulfurous acid (aq) + flouride ion (aq) <-> hydrogen flouride (aq) + hydrogen sulfite (aq) bisulfide (aq) + hydrogen cyanide (aq) <-> cyanide ion (aq) + hydrogen sulfide (aq)
If you mix equal concentrations of reactants and products, will the reaction proceed to the right...
If you mix equal concentrations of reactants and products, will the reaction proceed to the right or the left? HF (aq) + NO3- (aq) - HNO3(aq) +F- (aq) Match the items in the left column to the appropriate blanks in the sentences on the right Reset Help base .and is a stronger acid than Because proton transfer occurs from the stronger the reaction proceeds to the is a stronger base than to the stronger HNO, acid left right HF NO
the list of options are: acid, H30+, CH3OH, base, Br-, HO-, CH3O+H2, HBr, CH3Br, 15.7, -9,...
the list of options are: acid, H30+, CH3OH, base, Br-,
HO-, CH3O+H2, HBr, CH3Br, 15.7, -9, -1.7, H2O
Review Constants Periodic Table 1. Explain the difference in reactivity in substitution reactions between CH3Br and CH OH 2. Explain the difference in reactivity in substitution reactions between CH3 O H2 and CH3OH Match the words in the left column to the appropriate blanks in the sentences on the right. Make certain each sentence is complete before submitting your answer. Reset Help...
Tulung ate n illud aludke place in a single step. In the Sn2 reaction, the nucleophile...
Tulung ate n illud aludke place in a single step. In the Sn2 reaction, the nucleophile attacks the a-carbon from the backside and displaces the leaving group with an inversion of configuration occurring at the carbon. In the E2 elimination reaction, strong base removes an acidic hydrogen from the B-carbon and an alkene is formed as the leaving group is expelled from the a-carbon. This elimination follows Zaitsey's rule whereby the more substituted alkene is generally formed. In E2 elimination,...
Draw the major product of this reaction only. OTS acetone CH3 For the following reaction, which reaction will be faster (Left or Right)? Why? Click on the reaction that will be faster AND the right reason V1 + OH - or 1 + OOCCH3 Left Right Because the correct answer performs an elimination reaction while the incorrect one does a substitution reaction Because the correct answer has a stronger base than the incorrect answer. Resonance makes a stronger base. Because...
For the following reaction, which reaction will be faster (Left or Right)? Why? Click on the reaction that will be faster AND the right reason Br +CH OH — ory Br + CH, OH Left Right Because the correct reaction is SN1 and the incorrect reaction is E1. Substitution reactions are more stable than elimination reactions Because the correct reaction doesn't have a double bond. Double bonds make unstable carbocations Because the correct reaction has resonance. The resonance structures allow...
7. Which statement is true about the acid/base equilibrium reaction? ASH OH (A) The right side is favored because the base on the right side is the stronger of the two bases. (B) The right side is favored because the base on the right side is more stable. (C) The left side is favored because the base on the left side is weaker. (D) The right side is favored because we always draw reactions such that the right side is...
please answer all questions
The major product of this reaction is (4) CF NH. (B) CF (C) CF (D) no reaction CH, CH=24CH, beat The product of this rearrangement is (c) H 14 CH CHCH. (D) CH-CH2CH2 0.« *0. Which is not a reason this reaction fails to take place? (A) The C to which Cl is bonded is sp hybridized, making a shorter and stronger bond than those usually broken in substitution reactions. (B) Resonance gives the bond between...
When determining which mechanism (E1 or E2) occurs, the following process is helpful: 1) Determine the substitution (methyl, 1º, 2º, or 3“) of the alkyl halide 2) Determine the strength of the nucleophile Please fill out the following table, indicating the category of reaction (E1 or E2) that will occur in each set of alkyl halides and nucleophiles. If no reaction occurs, write 'NR: Alkyl Halide Strong Base Weak Base Methyl 1° 20 3° For each of the following reactions,...
If you mix equal concentrations of reactants and products, will the reaction proceed to the right or the left? HF (aq) + NO3- (aq) - HNO3(aq) +F- (aq) Match the items in the left column to the appropriate blanks in the sentences on the right Reset Help base .and is a stronger acid than Because proton transfer occurs from the stronger the reaction proceeds to the is a stronger base than to the stronger HNO, acid left right HF NO
the list of options are: acid, H30+, CH3OH, base, Br-,
HO-, CH3O+H2, HBr, CH3Br, 15.7, -9, -1.7, H2O
Review Constants Periodic Table 1. Explain the difference in reactivity in substitution reactions between CH3Br and CH OH 2. Explain the difference in reactivity in substitution reactions between CH3 O H2 and CH3OH Match the words in the left column to the appropriate blanks in the sentences on the right. Make certain each sentence is complete before submitting your answer. Reset Help...
Tulung ate n illud aludke place in a single step. In the Sn2 reaction, the nucleophile attacks the a-carbon from the backside and displaces the leaving group with an inversion of configuration occurring at the carbon. In the E2 elimination reaction, strong base removes an acidic hydrogen from the B-carbon and an alkene is formed as the leaving group is expelled from the a-carbon. This elimination follows Zaitsey's rule whereby the more substituted alkene is generally formed. In E2 elimination,...
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