(a)
Interpretation:
The rate constant for the decomposition of cyclobutane to ethylene at
Concept Introduction:
The temperature dependence of rate constant can be explained through Arrhenius equation.
Where
The logarithmic form of Arrhenius is given below.
Where,
(b)
Interpretation:
The cyclobutane concentration after two hours at
Concept Introduction:
The temperature dependence of rate constant can be explained through Arrhenius equation.
Where
The logarithmic form of Arrhenius is given below.
Where,
The integrated rate law for the first order reaction is given below.
Where,
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Chemistry: The Molecular Science
- What is/are the major product(s) of the following reaction? O AICI -Chts +arrow_forwardShown below is the major resonance structure for a molecule. Draw the second best resonance structure of the molecule. Include all non-zero formal charges. H. C H H C H :Ö: Click and drag to start drawing a structure.arrow_forwardShown below is the major resonance structure for a molecule. Draw the second best resonance structure of the molecule. Include all non-zero formal charges. H. C H H C. H H H H Click and drag to start drawing a structure. Xarrow_forward
- Relative Intensity Part VI. consider the multi-step reaction below for compounds A, B, and C. These compounds were subjected to mass spectrometric analysis and the following spectra for A, B, and C was obtained. Draw the structure of B and C and match all three compounds to the correct spectra. Relative Intensity Relative Intensity 100 HS-NJ-0547 80 60 31 20 S1 84 M+ absent 10 30 40 50 60 70 80 90 100 100- MS2016-05353CM 80- 60 40 20 135 137 S2 164 166 0-m 25 50 75 100 125 150 m/z 60 100 MS-NJ-09-43 40 20 20 80 45 S3 25 50 75 100 125 150 175 m/zarrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forwardPredicting the pro Predict the major products of this organic reaction. Explanation Check m ☐ + 5 1.03 Click and drag t drawing a stru 2. (CH₂)₂S 3 2 © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forward
- starting material target If so, draw a synthesis below. If no synthesis using reagents ALEKS recognizes is possible, check the box under the drawing area. Be sure you follow the standard ALEKS rules for submitting syntheses. + More... X Explanation Check C टे Br T Add/Remove step ☐ Br Br © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacarrow_forwardDon't used hand raitingarrow_forwardRelative Intensity Part VI. consider the multi-step reaction below for compounds A, B, and C. These compounds were subjected to mass spectrometric analysis and the following spectra for A, B, and C was obtained. Draw the structure of B and C and match all three compounds to the correct spectra. Relative Intensity Relative Intensity 100 HS-NJ-0547 80 60 31 20 S1 84 M+ absent 10 30 40 50 60 70 80 90 100 100- MS2016-05353CM 80- 60 40 20 135 137 S2 164 166 0-m 25 50 75 100 125 150 m/z 60 100 MS-NJ-09-43 40 20 20 80 45 S3 25 50 75 100 125 150 175 m/zarrow_forward
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