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11 Nov 2019

Please explain the structures step-by-step and in LEGIBLE writing. Currently taking Biochemistry, but confused as ever. Thank you.

6. Show how the following functional groups can be linked to one another. Give specific examples, full structures (of your choice) for the functional groups indicated and the "linked" products. 6. An aldehyde and two equivalents of an alcohol (2 equivalents) many other examples possible 6.2. Carbonate and two equivalents of an alcohol (2 equivalents)

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Casey DurganLv2

12 Mar 2019

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Â¥Write a brief (less than 150 words, 3 or 4 sentences) of the aim of the experiment

Â¥Address question of what was done, how it was done, and what compounds were used.

Â¥Include Chemical Reaction where relevant.

See text below. Please provide Purpose following the steps above. Thank you.

Alcohols R-O-H are characterized by the presence of the hydroxyl group

Because of intermolecular co-association, alcohols show higher boiling points

than aldehydes, ethers, or ketones of similar mass. Among alcohols, boiling

points increase with increased surface area. Increased surface area occurs as

more carbons are added to the alkyl portion or with decreased branching of th

alkyl group. Thus, 1-propanol has a higher boiling point than ethanol

(increased C#). 1-propanol also has a higher boiling point than 2-propanol

(decreased branching)

The solubility of alcohols in water decreases as the surface area of the

alkyl (nonpolar) portion increases. Thus, alcohols become less soluble in water

as the number of carbons in the alkyl group increases. When comparing

alcohols that contain the same number of carbons, branching of the alkyl group

decreases its surface area and thus increases the water solubility of the alcohol.

1-Propanol is slightly soluble in water while 2-propanol is quite soluble

The limit of water solubility is reached at about 4 or 5 carbons in the

alkyl group. However, it is possible to "salt out" or separate a water-soluble

alcohol from the water it is mixed with by the addition of certain salts such as

K2CO3. If an alcohol-water mixture is saturated with such a salt, the anion

selectively forms strong ion-dipole bonds to water, leaving the alcohol as a

separate layer. Thus, water is separated from the alcohol because the ionic salt

bonds more strongly with water than with the alcohol. There are twice as many

ion-dipole bonds possible with water than with the alcohol.

Alcohols are relatively acidic organic molecules, being weaker acids than

water, yet stronger than acetylene.

Acidity: water > alcohol > acetylene > ammonia > alkanes

Alcohols may be converted to sodium alkoxides by the action of metallic sodium

under anhydrous conditions. Primary alcohols react more readily tharn

secondary or tertiary alcohols due to the relative stability of the alkoxide ions in

the solvent alcohol.

R-o:-

Alcohols undergo nucleophilic substitution reactions with ease under

acidic conditions. The relative ease of such substitution for primary, secondary

and tertiary alcohols serves as a means of classification. Upon treatment with

concentrated HC1, tertiary alcohols are rapidly converted to alkyl chlorides

Secondary alcohols require warming in a boiling water bath for 15 minutes

Primary alcohols do not react at all under these conditions. The alkyl chlorides

formed by this reaction are insoluble in the concentrated HCl and form an

easily detectable second layer

R-O-H HC1 >

Ð-Ð-Ð

Complications arise from the fact that benzylic and allylic alcohols also

react immediately, but yield products that are soluble in the concentrated HCI

Alcohols are easily oxidized by any of these strong oxidizing agents:

dilute KMnO4, NajCr.07 in acid, or CrO3 (chromic anhydride)

acidified sodium dichromate is somewhat helpful in the classification of

alcohols. Prim

ary and secondary alcohols are oxidized rapidly within several

minutes, while tertiary alcohols do not react under these conditions

Oxidation occurs more easily when the carbon bearing the -OH group

bonded to at least one atom of hydrogen. The complex mechanism of

involves the transfer of a hydride ion H:- as a critical step.

hydrogen atom is absent (as in tertiary alcohols), no oxidation can occur

directly. Tertiary alcohols may be oxidized indirectly through the formation of

Alcohols which contain the partial structure C- CH3 give positive

Ð¾Ð½

results in the iodofora reaction. When the alcohol is dissolved in water and

KOH, the addition of a solution of 12 in KI yields a yellow precipitate of

iodoform, CHI3, along with the oxidized portion of the alcohol

Hypoiodite ion is produced by the reaction between molecular iodine and

hydroxide ion:

I2 + 4(OH) -

The hypoiodite ion in turn oxidizes an alcohol with the proper structure

Once this oxidation has occurred, additional hypoiodite ion continues to

react with the aldehyde or ketone produced:

CH,-C

3 (0I)-IC-c3 (OH)-

resulting in the final substitution reaction to give iodoform and the anion of a

carboxylic acid containing one carbon atom less than the original alcohol:

128

lodoform precipitates as fine yellow crystals. This precipitate, a result of a

specific oxidation followed by a substitution, is an indication of the partial

structure of the original alcohol.

Simple alcohols of up to ten carbon atoms may be detected by the

ammonium hexanitrocerrata(lV) reagent, (NH4Ce(NO,). The hexanitro-

cerrate(IV) ion has a distinctive orange-red color. When an alcohol, ROH is

added, one or more OR- groups replace the nitro groups as ligands in the

complex ion. The new complex ion formed has a distinctive color. The general

equation for this reaction is:

This test is positive for aliphatic alcohols up to approximately ten carbons in

length. Phenols or larger alcohols yield insoluble mixtures

Alcohols react with acids or with acid derivatives to form esters. This

characteristic reaction is useful in the formation of specific esters such as ethyl

acetate, acetylsalicylic acid (aspirin) and methyl salicylate (oil of wintergreen). In

this experiment, methyl salicylate will be prepared by reacting methyl alcohol

with salicylic acid in the presence of a trace of sulfuric acid as the catalyst

Lower molecular weight alcohols such as ethanol, methanol, and

isopropyi alcohol absorb water on exposure to moist air or are prepared as

azeotropic mixtures containing water. The presence of water in alcohols may be

detected in several ways. If a small lump of CaC2 is added to any alcohol that

contains a trace of water, a reaction occurs that produces immediate bubbles of

acetylene gas:

Thus, evolution of acetylene gas upon the addition of calcium carbide indicates

the presence of water in the alcohol. Another way to test for the presence of

water in alcohols involves the use of anhydrous cupric sulfate powder (CuSO4)

Anhydrous cupric sulfate is a very pale, almost white powder. In the presence of

water, deep blue crystals of cupric sulfate pentahydrate,

CuSO4-5H20, are formed. Thus, anhydrous cupric sulfate indicates the

presence of water in an alcohol by a simple color change.

Commercial ethanol is produced as an azeotropic mixture that contains

95% ethanol and 5% water. Absolute alcohol contains no water. Many reagent

grade alcohols are composed of a nonpotable mixture of 95% ethanol and 5%

isopropyl alcohol. Thus, absolute ethanol and reagent alcohols are both water

free and give negative results when tested for the presence of water

Please answer to the best of your ability

Show transcribed image text correctly.Completion and turning in of the entire review will result in an additional +3 pts on your final exam. Show all work to get extra credit. Please contact your instructor for clarification or specific questions. Report the following answers to the following problems with the correct number of significant figures and units: 1. 1 (0521 g 0.4953 0098 61â-24.135ë¯¸+1(120 64 g 4.1847 a)(21st-241530 1 (98.61 C-24.135)120.64g 4.1 21.5Â°C-24.153C) 0.0213548 moles b. (00020334-ern) + ((61210 goles Og) 0.002030 moles 1.02 moles (68.79 mlt29.901 ml) (26.3-0.230) c. 2. You are drying a sample of Bas(POsh. After 5 minutes of drying it weighs 1.2034 g. You continue to dry the sample for another 5 minutes and it now weighs 1.9346 g. What is the percent change in mass? 3. What is the percent mass of carbon in sodium carbonate? 4. What is the density of water at 23.1051Â°c? Use Table 1.1 on page 27 of your lab manual to help. 5. Based on the following reacts, predict the products. Write the balanced molecular equation, total ionic equation, and net ionic equation. All reactions are done in water a. Sodium chloride +silver (I) nitrate b. Calcium bromide + iron (III) sulfate c. Ammonium phosphate+ nickel (II) nitrate d. Hydrochloric acid+ calcium carbonate 6. Write the two balanced chemical reactions for a. Copper (II) oxide reacting with methane under high heat b. Copper (1) oxide reacting with methane under high heat 7. You analyze a mixed sample of copper (1) oxide and copper (II) oxide. The plot and trendline for mass of copper versus mass of mixture yields a slope of 0.8031. What are the mass percents of copper (0) oxide and copper (II) oxide in the mixture?
8. During week 1 of the Empirical Formula Lab you extinguished your "L-tube" flame without waiting 9. 20.00 ml of a 0.30 M potassium phosphate solution is combined with 20.00 mL of a 0.40 M solution 10. An Erlenmeyer flask is capped with a rubber stopper at room temperature (25 C) and atmospheric 11. The first step of the copper cycle lab was reacting solid copper with nitric acid. The copper ends up 12. What are the spectator ions in the 6 reactions performed during the copper cycle lab? for the reaction to cool and did NOT relight the "L-tube" flame. How would this affect your calculated percent mass compared to the true percent mass? of calcium chloride. What is the limiting reactant? What is the identity of the precipitate formed in the reaction? How many grams of product should be collected? pressure (1 atm). What temperature does the Erlenmeyer flask need to be heated to for the stopper to pop off? Assume it needs to exceed external pressure by 0.5 atm to release the stopper. oxidizing to copper (ll). What is the oxidizing reagent in this reaction? 13. The known specific heat capacity of aluminum is o g mo 25.316 g of aluminum is placed in 99.134 of water at a starting temperature of 22.45Â°C. The metal has a AT-84.02c what is the final 14. The AH, of cobalt (U) nitrate is +47.7 kJ/mol. What is the AHr of solid cobalt (1) nitrate? 15. 5.000 g of aluminum (Il) chloride is dissolved in 60.0 mL of water. The temperature changes by 16. Draw the Lewis dot symbols for the following atoms: temperature of the water? ÎÎ(Nouql)--205.00 kJ/mol ÎÎ,(Co2"m)--58.2 kJ/mol 0.331 Â°C. The specific heat capacity of aluminum (III) chloride is 0.903 Wat s AH.? what is ÎÎ a Ð°, Ð½Ðµ Ñ, Ñ c. Ar d. P e. H 17. Draw the Lewis structures for the following molecules: a. NHa b. O2 XeF d. NF

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