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)
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.
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
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…
Show how to convert cyclohexanol to these compounds. a. Cyclohexene b. Cyclohexane c. Cyclohexanone d. Bromocyclohexane
Which alcohol should be most soluble in a nonpolar solvent such as hexane, C6H14 ? a. CH3CH2CH2OH b. CH3CH2OH c. CH3CH2CH2CH2OH d. CH3OH e. CH3CH2CH2CH2CH2OH
Determine whether the alcohol is primary, secondary or tertiary. a. An alcohol rapidly evolved hydrogen gas when treated with sodium metal. It rapidly changed the color of potassium dichromate solution but did not form a cloudy layer when treated with ZnCl2 in HCl. b. An alcohol that did not evolve hydrogen gas and did not change the color of potassium dichromate solution but rapidly formed a cloudy layer when treated with concentrated ZnCl2 in HCl. c. An alcohol that evolved hydrogen gas at moderate speed and changed the color of potassium dichromate solution and formed a cloudy layer when treated with ZnCl2 in HCl