In organic reactions, according to the curved arrow notation , an arrow always originates from a negatively charged species or an electron rich species which means the tail of arrow starts from an electron rich species which attacks a positive species or site . So the head of an arrow will always point towards a species which is either bearing a positive charge or is electron deficient.
NOTE :
( In case of bonded electrons , the tail of arrow originates from the bonded electrons and the head of arrow points towards the species which takes away the bonded electrons . For example in case of Br leaving as Br- )
Question 1 1 pt (References) Draw curved arrows to indicate the movement of electrons in the...
Draw curved arrows to indicate the movement of electrons in the following reaction. HH н осн CH30: H-C-C-H — HC-C H Br Hн Arrow-pushing Instructions Not Submitted X OCH3 Hн CH30: Hccc-H Br C-CH Submit Answer Try Another Version 10 ltem attempts remaining Previous Cengage Learning Cengage Technical Support
draw curved arrows to show the movement of electrons in this step of the mechnaism. ХТ H но HаС. :он НаС. Hб CHз CHHЗ Hас Нас Next Previous :Br: Br: Cнз "CHз Hас HаС Br Н Н. -н Br н Br
Draw curved arrows to show the movement of electrons in this step of the mechanism. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions nga XT :00 Ph H3c-tö- PhẳNH H₃C N" H₃co CHỊ next Ph-NH2 H3Co PhNH - Ph—ŃHz CHỊ H3c-töl Ph–NH CH3 nggam '0 ' with the H₃C/ Ph Нsc H3COOH | Pháo: CH
Add curved arrows to the reactants to indicate the movement of electrons in this reaction. H ẲN–H :: H H
draw curved arrows to show the movement of electrons in this step of the reaction mechanism HCI H2O NH,CI -CEN ОН Acid catalyzed hydrolysis of a nitrile to give a carboxylic acid occurs by initial protonation of the nitrogen atom, fo Draw curved arrows to show the movement of electrons in this step of the reaction mechanism Arrow-pushing Instructions O: x H -CI: -NH₂ SLIDE ty Another Mansion 1 terrattuttomat
Chapter 6 Question 6 (References) 1 pt H Question 7 1 pt H Cl2 NaOH H H NaCl H2O Question 8 Н X) 1 pt H Question 9 © 1 pt O Question 101 pt H Question 11 1 pt Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Question 12 1 pt Arrow-pushing Instructions Question 13 1 pt Question 14 1 pt nn Question 15 1 pt Question 16 1 pt :cis...
Add curved arrows to the reactant side to illustrate the movement of electrons in the E2 reaction below. CHзн H3C H3C- + CH2 + :02H → = CH2 + :ö— H + Br: H3C 7 Hint Previous Check Answer Next Exit
Electrophilic addition of bromine, Br-, to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH2Cl2 In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due to steric clashes, the bromide ion always attacks the carbon from the opposite face of the bromonium ion so that a product...
Question 1 1 pt (References) CH3 Question 2 1 pt Question 3 1 pt CH3 Question 4 1 pt CH Question 5 1 pt When isopropylidenecyclohexane is treated with strong acid at room temperature, isomerization occurs in two steps to yield 1- isopropyleyclohexene. One of these steps is shown below; add curved arrows to the mechanism to indicate the movement of electrons in this step. Question 6 1 pt Question 7 Arrow-pushing Instructions pt atid no XT other H-CI CH3...
This nucleophilic substitution occurs with rearrangement. Draw curved arrows to show the movement of electrons in the following step of the reaction mechanism. NaOH HON Om This nucleophilic substitution occurs with rearrangement. Draw curved arrows to show the movement of electrons in the following step of the reaction mechanism. Arrow-pushing Instructions Nex mm 34 Submit Answer Try Another Version 1 item attempt remaining