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(a)
Interpretation: The given reactions are to be balanced.
Concept Introduction : According to the law of conservation of mass, the mass can neither be created nor to be destroyed. Every reaction must be balanced.
(a)
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Answer to Problem 5SP
The balanced equation is
Explanation of Solution
The unbalanced equation is given as:
The co-efficient of 3 is placed before
(b)
Interpretation: The given reactions are to be balanced.
Concept Introduction : According to the law of conservation of mass, the mass can neither be created nor to be destroyed. Every reaction must be balanced.
(b)
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Answer to Problem 5SP
The balanced equation is
Explanation of Solution
The unbalanced equation is given as:
The co-efficient of 3 is placed before
(c)
Interpretation: The given reactions are to be balanced.
Concept Introduction : According to the law of conservation of mass, the mass can neither be created nor to be destroyed. Every reaction must be balanced.
(c)
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Answer to Problem 5SP
The balanced equation is
Explanation of Solution
The unbalanced equation is given as:
The co-efficient of 2 is placed before
(d)
Interpretation: The given reactions are to be balanced.
Concept Introduction : According to the law of conservation of mass, the mass can neither be created nor to be destroyed. Every reaction must be balanced.
(d)
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Answer to Problem 5SP
The balanced equation is
Explanation of Solution
The unbalanced equation is given as:
The co-efficient of 2 is placed before
Chapter 11 Solutions
Chemistry 2012 Student Edition (hard Cover) Grade 11
- H3C H C=C CH3 H m-chloroperoxybenzoic acid CH2Cl2, rt C-C--. H3CH2CC H H3C CH3 Cl₂ H₂O NaOH H₂O D. S- E. CH3 H₂O₂, H₂O It CH₂O Na + CHI F. HI, H₂O heat G. 4 OH CH3CHCH3 + ICH2CH3 1. NaH (CH3)3COH (CH3)3 COCHCH2CH3 2. CH3arrow_forward5. Show how the ether below could be prepared from toluene and any other necessary reagents. Show all reagents and all intermediate structures. H3C- H3C- CI OCH2CH3arrow_forwardGiven 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_forward
- Please 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_forwardEstimation 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_forward
- Draw 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_forwardPropose 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_forward
- Provide 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_forwardQ2. 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_forward
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