The validation of the fact that addition of HCl is not a stereospecific reaction by using cis and trans hex − 3 − ene is to be stated. The structure of the stereoisomers formed from the given reaction is to be drawn. Concept introduction: Electrophilic addition reaction follows Markovnikov rule. According to Markovnikov’s rule, the positive part of halogen acid attached to that carbon atom in C=C bond which carries higher number of hydrogen atoms and the negative part of halogen acid will attach to that carbon atom in C=C bond which has lesser number of hydrogen atoms. A compound exhibits stereoisomers when it contains more than one stereogenic centers. The maximum number of stereoisomers a compound with n number of stereogenic centers can show is 2 n . A carbon atom which is bonded to four different groups is termed as chiral center or stereogenic center.
The validation of the fact that addition of HCl is not a stereospecific reaction by using cis and trans hex − 3 − ene is to be stated. The structure of the stereoisomers formed from the given reaction is to be drawn. Concept introduction: Electrophilic addition reaction follows Markovnikov rule. According to Markovnikov’s rule, the positive part of halogen acid attached to that carbon atom in C=C bond which carries higher number of hydrogen atoms and the negative part of halogen acid will attach to that carbon atom in C=C bond which has lesser number of hydrogen atoms. A compound exhibits stereoisomers when it contains more than one stereogenic centers. The maximum number of stereoisomers a compound with n number of stereogenic centers can show is 2 n . A carbon atom which is bonded to four different groups is termed as chiral center or stereogenic center.
Solution Summary: The author explains the structure of the stereoisomer formed from the electrophilic addition reaction.
Definition Definition Organic compounds that contain at least one double bond between carbon-carbon atoms. The general molecular formula for alkenes with one double bond is C n H 2n .
Chapter 10, Problem 10.55P
Interpretation Introduction
Interpretation: The validation of the fact that addition of HCl is not a stereospecific reaction by using cis and trans hex−3−ene is to be stated. The structure of the stereoisomers formed from the given reaction is to be drawn.
Concept introduction: Electrophilic addition reaction follows Markovnikov rule. According to Markovnikov’s rule, the positive part of halogen acid attached to that carbon atom in C=C bond which carries higher number of hydrogen atoms and the negative part of halogen acid will attach to that carbon atom in C=C bond which has lesser number of hydrogen atoms.
A compound exhibits stereoisomers when it contains more than one stereogenic centers. The maximum number of stereoisomers a compound with n number of stereogenic centers can show is 2n. A carbon atom which is bonded to four different groups is termed as chiral center or stereogenic center.
A complete tensile test was performed on a magnesium
specimen of 12 mm diameter and 30 mm length, until breaking.
The specimen is assumed to maintain a constant volume.
Calculate the approximate value of the actual stress at breaking.
TABLE. The tensile force F and the length of the specimen are
represented for each L until breaking.
F/N
L/mm
0
30,0000
30,0296
5000
10000 30,0592
15000 30,0888
20000
30,15
25000 30,51
26500
30,90
27000
31,50
26500
32,10
25000 32,79
None
Differentiate between plastic deformation, elastic deformation, viscoelastic deformation and viscoplastic deformation.