Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

Write a structural formula for each compound. (a) Isopropyl alcohol (b) Propylene glycol (c) 5 -Methyl-2-hexanol (d) 2 -Methyl-2-propyl-1,3-propanediol (e) 1-Chloro-2-hexanol (f) cis-3-Isobutylcyclohexanol (g) 2,2-Dimethyl-1-propanol (h) 2-Mercaptoethanol (i) Allyl alcohol (j) trans-2-Vinylcyclohexanol (k) (Z) -5-Methyl-2-hexen-1-ol (1) 2-Propyn-1-ol (m) 3-Chloro-1,2-propanediol (n) cis-3-Pentene-1-ol

Short Answer

Expert verified
Question: Give the structural formulas for the following organic compounds: (a) Isopropyl alcohol (b) Propylene glycol (c) 5-Methyl-2-hexanol (d) 2-Methyl-2-propyl-1,3-propanediol (e) 1-Chloro-2-hexanol (f) cis-3-Isobutylcyclohexanol (g) 2,2-Dimethyl-1-propanol (h) 2-Mercaptoethanol (i) Allyl alcohol (j) trans-2-Vinylcyclohexanol (k) (Z)-5-Methyl-2-hexen-1-ol (l) 2-Propyn-1-ol (m) 3-Chloro-1,2-propanediol (n) cis-3-Pentene-1-ol Answer: (a) CH3-CH(OH)-CH3 (b) CH2(OH)-CH(OH)-CH3 (c) CH3-CH2-CH(OH)-CH2-CH(CH3)-CH3 (d) CH3-CH2-CH(OH)-C(CH3)(CH3)-CH2(OH) (e) Cl-CH2-CH(OH)-CH2-CH2-CH2-CH3 (f) See the structural formula drawn in the solution above. (g) CH3-CH(OH)-C(CH3)2 (h) HS-CH2-CH2(OH) (i) OH-CH2-CH=CH2 (j) See the structural formula drawn in the solution above. (k) CH3-CH2-CH=CH-CH(CH3)-CH2OH (Z configuration) (l) CH3-C≡C-OH (m) CH2(OH)-CH(OH)-CH2Cl (n) CH2(OH)-CH2-CH=CH-CH3 (cis configuration)

Step by step solution

01

(a) Isopropyl alcohol

Isopropyl alcohol is an alcohol (OH group) attached to an isopropyl radical (CH3-CH-). To write the structural formula: CH3-CH(OH)-CH3
02

(b) Propylene glycol

Propylene glycol is a diol (two OH groups) derived from propylene. To write the structural formula: CH2(OH)-CH(OH)-CH3
03

(c) 5-Methyl-2-hexanol

5-Methyl-2-hexanol is a hexanol (6-carbon chain with an OH group) with a methyl group (CH3) on the 5th carbon. To write the structural formula: CH3-CH2-CH(OH)-CH2-CH(CH3)-CH3
04

(d) 2-Methyl-2-propyl-1,3-propanediol

2-Methyl-2-propyl-1,3-propanediol is a propanediol (3-carbon chain with two OH groups) with a methyl and propyl group at the 2nd carbon. To write the structural formula: CH3-CH2-CH(OH)-C(CH3)(CH3)-CH2(OH)
05

(e) 1-Chloro-2-hexanol

1-Chloro-2-hexanol is a hexanol (6-carbon chain with an OH group) with a chlorine atom on the 1st carbon. To write the structural formula: Cl-CH2-CH(OH)-CH2-CH2-CH2-CH3
06

(f) cis-3-Isobutylcyclohexanol

cis-3-Isobutylcyclohexanol is a cyclohexanol (cyclohexane with an OH group) with an isobutyl group on carbon 3 in a cis configuration. To write the structural formula: (OH) (CH3) | | | -CH | | -CH-CH-CH-CH- | | -CH-CH-CH2- (with CH3)-(CH2-)-(CH3) groups in cis configuration with -OH group
07

(g) 2,2-Dimethyl-1-propanol

2,2-Dimethyl-1-propanol is a propanol (3-carbon chain with an OH group) with two methyl groups on the 2nd carbon. To write the structural formula: CH3-CH(OH)-C(CH3)2
08

(h) 2-Mercaptoethanol

2-Mercaptoethanol is an ethanol (two-carbon chain with an OH group) with a thiol (SH group) on the 2nd carbon. To write the structural formula: HS-CH2-CH2(OH)
09

(i) Allyl alcohol

Allyl alcohol is an alcohol (OH group) attached to an allyl group (CH2-CH=CH2). To write the structural formula: OH-CH2-CH=CH2
10

(j) trans-2-Vinylcyclohexanol

trans-2-Vinylcyclohexanol is a cyclohexanol with a vinyl group (CH=CH2) on the 2nd carbon in a trans configuration. To write the structural formula: (OH) (CH3) | | | -CH | | -CH-CH-CH-CH- | | -CH-CH-(=CH2) (trans configuration with -OH group)
11

(k) (Z)-5-Methyl-2-hexen-1-ol

(Z)-5-Methyl-2-hexen-1-ol is a hexenol with an OH group on the 1st carbon and a methyl group on the 5th carbon. The double bond has a Z stereochemical configuration. To write the structural formula: CH3-CH2-CH=CH-CH(CH3)-CH2OH (Z configuration)
12

(i) 2-Propyn-1-ol

2-Propyn-1-ol is a propynol (3-carbon chain with an OH group and a triple bond). To write the structural formula: CH3-C≡C-OH
13

(m) 3-Chloro-1,2-propanediol

3-Chloro-1,2-propanediol is a propanediol (3-carbon chain with two OH groups) with a chlorine atom on the 3rd carbon. To write the structural formula: CH2(OH)-CH(OH)-CH2Cl
14

(n) cis-3-Pentene-1-ol

cis-3-Pentene-1-ol is a pentene with an OH group on the 1st carbon and a double bond on carbon-3 in a cis configuration. To write the structural formula: CH2(OH)-CH2-CH=CH-CH3 (cis configuration)

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Using your roadmap as a guide, show how to convert butane into 2 -butanone. Show all reagents and all molecules synthesized along the way.

Write equations for the reaction of 1-butanol with each reagent. Where you predict no reaction, write NR. (a) Na metal (b) \(\mathrm{HBr}\), heat (c) \(\mathrm{HI}\), heat (d) \(\mathrm{PBr}_{3}\) (e) \(\mathrm{SOCl}_{2}\) pyridine (f) \(\mathrm{K}_{2} \mathrm{Cr}_{2} \mathrm{O}_{7}, \mathrm{H}_{2} \mathrm{SO}_{4}, \mathrm{H}_{2} \mathrm{O}\), heat (g) \(\mathrm{HIO}_{4}\) (h) \(\mathrm{PCC}\) (i) \(\mathrm{CH}_{3} \mathrm{SO}_{2} \mathrm{Cl}\), pyridine (j) \(\mathrm{CO}_{2} \mathrm{Cl}_{2}\) and \(\mathrm{DMSO}\), followed by triethylamine (k) DMP (i) triethylamine

Compounds that contain an \(\mathrm{N}-\mathrm{H}\) group associate by hydrogen bonding. (a) Do you expect this association to be stronger or weaker than that of compounds containing an \(\mathrm{O}-\mathrm{H}\) group? (b) Based on your answer to part (a), which would you predict to have the higher boiling point, 1 -butanol or 1 -butanamine?

The decalinols A and B can be equilibrated using aluminum isopropoxide in 2 -propanol (isopropyl alcohol) containing a small amount of acetone. Assuming a value of \(\Delta G^{0}\) (equatorial to axial) for cyclohexanol is \(4.0 \mathrm{~kJ}(0.95 \mathrm{kcal}) / \mathrm{mol}\), calculate the percent of each decalinol in the equilibrium mixture at \(25^{\circ} \mathrm{C}\).

Propose a mechanism for the following pinacol rearrangement catalyzed by boron trifluoride ethyl etherate.

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free