Docsity
Docsity

Prepare for your exams
Prepare for your exams

Study with the several resources on Docsity


Earn points to download
Earn points to download

Earn points by helping other students or get them with a premium plan


Guidelines and tips
Guidelines and tips

Organic Chemistry I: Alkenes Exercise, Assignments of Organic Chemistry

A chemistry exercise focusing on identifying the number of unsaturations in given molecular formulas, naming alkenes according to iupac rules, and determining the geometry and conformational isomers of alkenes. It also includes questions on the formation of c=c π bonds, saytzeff's rule, and bredt's rule.

Typology: Assignments

Pre 2010

Uploaded on 08/18/2009

koofers-user-l9z
koofers-user-l9z 🇺🇸

10 documents

1 / 2

Toggle sidebar

This page cannot be seen from the preview

Don't miss anything!

bg1
Name: . . . . . . .. . . . . . . Date: . . . . . .. . . . .
DEPARTMENT OF BIOLOGICAL AND PHYSICAL SCIENCEA
Phone: (803) 536-8513 and 536-7105
FAX: (803) 536-4685 & 536-8436
Organic Chemistry I, C306: Alkenes
Choose the one alternative that best completes the statement or answers the question.
1) How many elements of unsaturation are implied by the molecular formula below?
(I) C6H12? A) 0 B) 1 C) 2 D) 3 E) 4
(II) C5H5NO2? A) 0 B) 1 C) 2 D) 3 E) 4
2) What two atomic orbitals or hybrid atomic orbitals overlap to form the C=C π bond in ethylene?
A) C sp3 + C sp3 B) C sp3 + C sp2 C) C p + C p D) C sp2 + C p E) C sp2 + C sp2
3) Using Saytzeff's rule, choose the most stable alkene among the following.
A) 4-methylcyclohexene B) 3-methylcyclohexene C) 1-methylcyclohexene
D) They are all of equal stability according to Saytzeff's rule.
Write your answer in the space provided or on a separate sheet of paper.
4) Provide the proper IUPAC name for the alkene shown below.
(I) CH=CHCH2CH2CH2CH3
…………………………
............................................
…………………..
....................................................
……………………...
5) Draw an acceptable structure for:
1,2-dimethylcyclohexene. (Z)-2-chloro-4-ethylhex-2-ene. 4-phenylbut-1-ene.
6) Describes the geometry (E or Z) about the carbon-carbon double bond in the alkenes below?
7) Does the alkene shown below violate Bredt's rule? explane for each
8) Draw and name all alkenes which have the molecular formula C6H12
pf2

Partial preview of the text

Download Organic Chemistry I: Alkenes Exercise and more Assignments Organic Chemistry in PDF only on Docsity!

Name:...... ........ Date:..... ......

DEPARTMENT OF BIOLOGICAL AND PHYSICAL SCIENCEA

Phone: (803) 536-8513 and 536-

FAX: (803) 536-4685 & 536-

Organic Chemistry I, C306: Alkenes

Choose the one alternative that best completes the statement or answers the question.

  1. How many elements of unsaturation are implied by the molecular formula below?

(I) C6H

? A) 0 B) 1 C) 2 D) 3 E) 4

(II) C

H5NO2? A) 0 B) 1 C) 2 D) 3 E) 4

  1. What two atomic orbitals or hybrid atomic orbitals overlap to form the C=C π bond in ethylene?

A) C sp

  • C sp B) C sp
  • C sp C) C p + C p D) C sp
  • C p E) C sp
  • C sp
  1. Using Saytzeff's rule, choose the most stable alkene among the following.

A) 4-methylcyclohexene B) 3-methylcyclohexene C) 1-methylcyclohexene

D) They are all of equal stability according to Saytzeff's rule.

Write your answer in the space provided or on a separate sheet of paper.

  1. Provide the proper IUPAC name for the alkene shown below.

(I) CH=CHCH2CH2CH2CH

  1. Draw an acceptable structure for:

1,2-dimethylcyclohexene. ( Z )-2-chloro-4-ethylhex-2-ene. 4-phenylbut-1-ene.

  1. Describes the geometry (E or Z) about the carbon-carbon double bond in the alkenes below?

  2. Does the alkene shown below violate Bredt's rule? explane for each

  3. Draw and name all alkenes which have the molecular formula C 6

H

12

9)Draw all likely alkene products in the following reactions and circle the product you expect to predominate.

Write a detailled mechanism for each producat that you would expect (5 point each).

  1. Propose a detailed, step-by-step mechanism for the reaction pathway shown below.