Please help me with these questions. Thanks! Functions:11. (a) Circle the location(s) atwhich these reactants willнннн(b).Н-с-с-о-НН-с-с-о-Нcombine. (b) Name the typeof reaction. (c) Name theнн(c)+class of compound produced.12. (a) Circle the location(s) atwhich these reactants willнн(b)combine. (b) Name the typeof reaction. (c) Name theclass of compound produced.Н—СН-С-с-о-Н(c)HOHнн+ 13. What is the practical application of the reaction in #11? How do we use the products of this type ofreaction? Explain your ideas and provide two different examples of these materials.14. What is the practical application of the reaction in #12? How do we use the products of this type ofreaction? Explain your ideas and provide two different examples of these materials.15. What is the difference between a primary alcohol and a tertiary alcohol? Explain the key structuraldifferences and provide one example of each type of organic compound.16. Your chemistry partner tells you about an organic compound called 2-propyl-3-methyl-4-octene. You aresure this name is incorrect. What do you tell your chemistry partner? Explain two key points.

Note:- according to our guidelines we are supposed to answer only one question

11. (a) Circle the location(s) at нн нн which these reactants will (b), Н-С-с-О-Н Н-с-с-о-н (c) combine. (b) Name the type нн нн of reaction. (c) Name the class of compound produced. +

11. (a) Circle the location(s) at нн нн which these reactants will (b), Н-С-с-О-Н Н-с-с-о-н (c) combine. (b) Name the type нн нн of reaction. (c) Name the class of compound produced. +

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter22: Organic And Biological Molecules

Section: Chapter Questions

Problem 5RQ: What functional group distinguishes each of the following hydrocarbon derivatives? a....

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5. Draw the structure of each of the following alcohols. Then draw and name the product you would expect to produce by the oxidation of each. a. 4-Methyl-2-heptanol b. 3,4-Dimethyl-1-pentanol c. 4-Ethyl-2-heptanol d. 5,7-Dichloro-3-heptanol
1. The acid-catalyzed elimination of an alcohol is an equilibrium reaction and requires special reac- tion conditions to favour the formation of the alkene product. What chemical principle controls the amount of alkene product that is produced? Provide two laboratory techniques that can be used to obtain good alkene yields in alcohol elimination reactions.
Which of the following reactions can be used to make the following alcohol? OH 1. LIAIH4, ether 2. H30* 1. OsO4 2. NaHSO3, H20 1. CH3CH2MgBr, ether H. 2. H3O*, H2O 1. Hg(OAc)2, H2O/THF 2. NABH4 MacBook Pro
10.The reaction of excess Grignard reagent with an ester of formic acid, HCO2R, gives a. methanol. b.a tertiary alcohol. c. primary alcohol d.secondary alcohol.
10. What product(s) would result from the oxidation of each of the following alcohols with, for example, potassium permanganate? If no reaction occurs, write N.R. a. 2-Butanol b. 2-Methyl-2-hexanol c. Cyclohexanol d. 1-Methyl-1-cyclopentanol
Please help me with this Explain these reactions of alcohol (organic chemistry) 1. Substituition 2. Esterfication 3. Dehydration 4. Oxidation Then please write about the types of reactions for ethers (organic chemistry)
Write the structure of the product formed in the following oxidation-reduction reactions. Label the functional group in the reactant that changes, and identify the new functional group in the product. If the functional group is an alcohol, identify the type of alcohol. If there is no reaction, state so. 54 Ac a. H. ОНН Н [O] Н-С-С—С-С-Н of H. ННН b. НННС 84 Н-С-С-С--С--Н ННН C. НННН [0] form НО-С-С-С-С-Н H HH H Hd. HO [H] pertortm e. [0] ОН কন
11. Alkenes are common starting organic compounds used to make other useful compounds. a. Start with any alkene. Choose two of the reactions you have learned about that use alkenes as a reactant. You may use any other chemicals you feel necessary. Then, compare and contrast the products made from these reactions.
Consider the following reactions: a. When C6H14 is reacted with Br2(g) in the presence of ultraviolet light, four different monobromination products form. What is the structure of C6H14 in this reaction? b. When CSH10 is reacted with H2O, a tertiary alcohol is produced as the major product. What is the structure of C5H10 in this reaction? When C6H10 is reacted with HCI, 1-chloro-1-methylcyclopentane is produced as the major product. What are the two possible structures for C6H10 in this С. reaction? d. When a hydrocarbon is reacted with water and the major product of this reaction is then oxidized, cyclohexanone is produced. What is the structure of the hydrocarbon in this reaction? When C4H100 is oxidized, a carboxylic acid is produced. What are the possible е. structures for C4H100 in this reaction?
7. What is the major organic product obtained from the following reaction? a. 1 b. 2 c. 3 d. 4 CH3 1. BH3 2. H₂O2. NaOH CH3 CH3 H3C OH HO CH3 OH "OH OH 3
10. How many H-bonds can a secondary alcohol form? A. 3 B. 1 C. 2 D. 0
1. Consider the solubility and boiling point of the following pair of compounds: n-butyl alcohol and diethyl ether. The boiling points for the compounds are 118 °C and 35 °C respectively. The solubility for both compounds is the same (8g/100g water). Explain this observation for (i) boiling point disparity; (ii) solubility similarity a. H-bonds form in diethyl ether; n-butyl alcohol forms H-bonds in water b. H-bonds form in n-butyl alcohol; diethyl ether forms H-bonds in water c. H-bonds in n-butyl alcohol; Both compounds form H-bonds in water d. Both compounds form H-bonds; Both compounds form H-bonds in water 2. Account for the bond angle differences between (i) H-C-H (109.5°) in methane and H-S-H (90°); H-C-H (109.5°) and H-O-H (107.5°) in water. a. The H-S-H has two lone pairs; The H-O-H has two lone pairs b. The H-S-H has no hybridization at p-orbitals; The H-O-H has two lone pairs c. The H-S-H has two lone pairs; The H-O-H has no hybridization…