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10 Nov 2019

Addition to Conjugated DienesConjugated dienes are molecules in which there are two double bonds separated by one single bond. This orientation of double bonds increases the stability of the molecules in comparison to similar alkane or alkene molecules. Conjugated dienes can participate in many of the same addition reactions as their alkene counterparts.Part AThe first step of an addition to a conjugated diene involves the addition of an electrophile to form a resonance stabilized allylic cation. Draw both resonance structures of the allylic cation formed when one molecule of adds to the symmetrical diene, 3,4-dimethylhexa-2,4-diene.

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5 Feb 2019

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1. Which of the following reagent(s) can be used to prepare a mixture of o and p-nitro toluene from toluene

(A) HNO₂ (B) HNO₃ (C) HNO₃/Fe (D) HNO₃/H₂SO₄ (E) NaNO₂

(A) H₂SO₃ (B) SO₃/ Which of the following reagent(s) can be used to convert nitrobenzene to m-nitrobenzenesulfonic acid Fe (C) H₂SO₃/Fe (D) H₂SO₄/Al₂(SO₄)₃ (E) H₂SO₄.SO₃

3. Which of the following reagent(s) can be used to prepare bromobenzene from benzene

(A) NBS (B) Br₂/FeBr₃ (C) H₂SO₄/Br₂ (D) Br₂/AlBr₃ (E) Br₂/Pd

4. Which of the following functional groups are o,p-directing ?

(A) Br, CH₂CH₃, NH₂ (B) Cl, NH₂, COOH (C) I, SO₃H, OH (D) OCH₃, Cl, COCH₃ (E) NO₂, CH₃, OH

5. Which of the following reagent(s) gives the reaction below

(A) CH₃Cl (B) Cl₂/ Fe (C) Cl₂/ AlCl₃ (D) Cl₂/ FeCl₃ (E) Cl₂/ HCl

6. Friedal-Craft acylation reagent(s)

(A) CH₃Cl/AlCl₃ (B) Cl₂/CH₃COCl (C) CH₃COCl/AlCl₃ (D) CH₃COCl/FeCl₃ (E) CH₃Cl/FeCl₃

7. Which of the following functional groups are m-directing ?

(A) NO₂, CH₃, OH (B) Br, NH₂, COOH (C) I, SO₃H, OH (D) OCH₃, Cl, COCH₃ (E) COCH_3, SO₃H, CHO

8. Which of the following compound can be used in the Diels-Alder reaction

(A) 2-methyl, 2,4-hexadiene (B) 2,5-hexadiene (C) 1-methyl,cyclohexa-1,4-diene (D) cyclohexa-1,4-diene

(E) 2-methyl, 1,5-hexadiene

9. Which statement about benzene is incorrect?

(A) The Cï¿½C p - bonding is delocalized (B) The C₆ ring is planar (C) The average C - C bond distance is the same as C-C double bonds (D) Each C atom is sp² hybridized ( E ) There are 12 s (sigma) bonds in benzene

10. Which of the following is NOT aromatic

(A) Cyclopropenyl cation (C₃H₃⁺) (B) Benzene (C₆H₆) (C) [16]-Annulene (C₁₆H₁₆)

(D) Cycloheptatrienyl cation (C₇H₇⁺) (E) [18]-Annulene (C₁₈H₁₈)

11. Conjugate addition of one equivalent of deuterium bromide (DBr) to 1,3-butadiene gives

(A) 3-bromo, 4-deutero, 1-butene (B) 3-bromo, 4-deutero, 2-butene (C) 4-bromo, 3-deutero, 1-butene (D) 1-bromo, 4-deutero, 2-butene (E) 1-bromo, 4-deutero, 1-butene

12. Which of the following is a conjugated diene

(A) cyclopentadiene (B) 2-methylcyclohexanone (C) 1-methyl,cyclohexa-1,4-diene (D) cyclohexa-1,4-diene

(E) cycloocta-1,5-diene

13. The aromatic compound is

14. Which of the following reaction involves a benzyne mechanism ?

(A) Ph-CH₃ ? Ph-COOH (B) Ph-CH₃ ? Ph-CHO (C) Ph-OH ? Ph-Cl (D) Ph-Cl ? Ph-OH

(E) none of these

15. Which of the following reagent(s) can be used to prepare a mixture of o and p-nitro toluene from

toluene

(A) HNO₂ (B) HNO₃ (C) HNO₃/Fe (D) HNO₃/H₂SO₄ (E) NaNO₂

16. Friedal-Craft alkyation reagent(s)

(A) C₂H₅Cl/AlCl₃ (B) Cl₂/CH₃COCl (C) CH₃COCl/AlCl₃ (D) CH₃COCl/FeCl₃ (E) CH₃Cl/FeCl₃

17. Which of the following functional groups are o,p-directing ?

(A) NO₂, SO₃H, CHO (B) Br, NH₂, COOH (C) I, OH, CH₃ (D) OCH₃, Cl, COCH₃ (E) COCH_3, SO₃H, Br

18. Major product in the reaction of benzene with 1-bromopropane, in the presence of AlBr₃ catalyst

(A) bromobenzene (B) n-propylbenzene (C) iso-propylbenzene (D) o-bromo-n-propylbenzene

(E) p-bromo-n-propylbenzene

19. Which of the following is the electrophile in the nitration reaction

(A) ⁺HNO₂ (B) NO₂⁺ (C) N₂+ (D) HNO₃/H₂SO₄ (E) NO₃⁺

20. Which of the following is the electrophile in the sulfonation reaction

(A) ⁺HSO₂ (B) SO₂⁺ (C) SO₃⁺ (D) SO₃/H₂SO₄ (E) HSO₃⁺

21. Which of the following is the electrophile in the Friedel-Craft acylation reaction

(A) RCO₂⁺ (B) RCO⁺ (C) CO₂⁺ (D) RX/H₂SO₄ (E) RCO₃⁺

22. The benzyne intermediate has ï¿½ï¿½ p bonds

(A) 1 (B) 2 (C) 3 (D) 4 (E) 5

23. The reagent used for Allylic/benzylic bromination is:

(A) NBS (B) Br₂/ Fe (C) Br₂/ AlBr₃ (D) Br₂/ FeBr₃ (E) Br₂/ HBr

24. Which of the following is an oxidation reagent

(A) H₂SO₄ (B) KMnO₄ (C) KMnO₂ (D) NaBH₄ (E) AlCl₃

25. The formula of fuming sulfuric acid

(A) H₂SO_4.SO₃ (B) H₂SO_4.SO₂ (C) H₂SO_4.HSO₂ (D) H₂SO_4.HSO₃ (E) H₂SO_4.SO

26. How do you prepare the following compounds, starting from benzene ?

(a). aniline (b). Iodo benzene (c). benzoic acid (d). benzylbromide (e). m-methyl benzoic acid

(f). p-nitrobenzoic acid (g) m-nitrobenzoic acid (h). p-chlorobenzenesulfonic acid (i). m-chlorobenzenesulfonic

acid (j) 3-isopropyl benzoic acid (k). 4-isopropyl toluene

27. Draw the product(s) from the following reactions showing the mechanisms

(a) 1,3-butadiene with acrylonitrile

(b) 1,3-butadiene with one eqv. HBr

(d) 1,3-cyclohexadiene with one eqv. HBr

(e) 1,3-cyclohexadiene with two eqv. HBr

(f) cyclopentadiene with two eqv. HBr

28. How do you prepare the following compounds, starting from toluene ?

(a). benzoic acid (b). benzyl alcohol (c). m-bromobenzoic acid (d). m-methylbenzoic acid (e). m-nitro

benzoic acid (f). p-nitrobenzoic acid

29. What is/are the product(s) expected when ethylbenzene is reacted with

(a). NBS

(b). Br₂/FeBr₃

(c). KMnO₄, then H⁺

(d). fuming H₂SO₄

(e). NBS, then aq. NaOH

(f) iso-butylbromide/AlBr₃

lilacwater-buffalo25

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

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