(a)
Interpretation:
The given reaction has to be balanced using the smallest whole number coefficient, and the expression for
Concept Introduction:
The equilibrium constant,
For the reaction,
The equilibrium constant can be written as
(a)
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Explanation of Solution
The given reaction is
In the reaction, chlorine and hydrogen are unbalanced.
Chlorine can be balanced as
The reaction is balanced completely. The complete balanced reaction is given as
The equilibrium constant of the reaction can be written by taking the partial pressures of products on numerator, raised to a power of its
The equilibrium constant expression is written as
(b)
Interpretation:
The given reaction has to be balanced using the smallest whole number coefficient, and the expression for
Concept Introduction:
Refer to sub-part (a).
(b)
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Explanation of Solution
The given reaction is
Nitrogen, hydrogen, chlorine and fluorine are unbalanced in the reaction.
Nitrogen can be balanced as
Chlorine can be balanced as
Fluorine is balances as
Now, the hydrogen’s in reaction are also balanced and the balanced reaction is given as
The equilibrium constant expression is written as
(c)
Interpretation:
The given reaction has to be balanced using the smallest whole number coefficient, and the expression for
Concept Introduction:
Refer to sub-part (a).
(c)
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Explanation of Solution
The given reaction is
Oxygen is unbalanced in the reaction.
Oxygen can be balanced as
Now, nitrogen has to be balanced. The balanced reaction is
The equilibrium constant expression is written as
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Chapter 5 Solutions
CHEM PRINCIPLES LL W/ACHIEVE ONE-SEM
- Given the major organic product(s) of each of the following reactions. If none is predicted, write "N.R." [answer 61 a. b. H3C C. NO₂ CH3CH2CH2Cl AICI 3 1) NaOH CI 2) H3O+ NO₂ 1. SnCl2, H3O+ 2. NaOH 3arrow_forwardPlease correct answer and don't used hand raitingarrow_forwardTo answer the following questions, consider the reaction below: CH3 . CH3 OH a. The best reagents for accomplishing the above transformation are.... a. 1. OsO4, pyridine 2. NaHSO3, H₂O b. 1. Hg(OAc)2, H₂O 1. C. 2. NaBH4 RCO₂H, CH2Cl₂ 2. H₂O* d. 1. BH3, THF 2. H₂O₂, OH b. The alcohol product is classified as a: a. 1° alcohol b. 2° alcohol C. 3° alcohol d. 4° alcohol c. The conversion of an alcohol into an alkyl chloride by reaction with SOCI2 is an example of: a. b. ن نخنه C. d. an El process an Syl process an E2 process an Sy2 processarrow_forward
- Estimation of ash in food Questions: Q1: What does the word ash refer to? Q2: Mention the types of ash in food Q3: Mention the benefit of using a glass dryerarrow_forwardDraw structures corresponding to the names given a. m-fluoronitrobenzene b. p-bromoaniline c. o-chlorophenol d. 3,5-dimethylbenzoic acidarrow_forwardIllustrate the reaction mechanism the following reactionarrow_forward
- Propose a synthesis for the following compound using benzene or toluene and any other reagents necessary. Show all major intermediate compounds that would probably be isolated during the course of your synthesis. on. Harrow_forwardProvide correct IUPAC names for each of the following compounds. NOT a. b. C. 2003 H,N- CH3 NH2 CHarrow_forward. Consider the reaction below to answer the following questions. OH 1. NaH 2. CH3I, ether O-CH3 A. Write the complete stepwise mechanism for the reaction. Show all intermediate structures and all electron flow with arrows. B. Mechanistically, the Williamson ether synthesis outlined above is: ن نخنه a. an El process b. an SN1 process C. an E2 process d. an SN2 process C. Alternatively, cyclopentyl methyl ether may be synthesized from cyclopentene. synthesis of cyclopentyl methyl ether from cyclopentene. Outline aarrow_forward
- Q2. A good synthesis of (CH3)3C- would be: A) B) CSI3 0 CH3CC1 (CH3) 3CC1 Benzene AlCl3 AlCl3 (CH3)3CC1 CH3CC1 Benzene C) AlCl3 0 AlCl3 CH3CC1 (CH3) 2C-CH2 Bonzone AlCl3 HF D) More than one of these E) None of thesearrow_forwardDon't used hand raiting and correct answer and don't used Ai solutionarrow_forwardShow how you might carry out the following transformation or reactions: toluene to m-chlorobenzoic acidarrow_forward
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