Arrow-pushing Instructions nne PhP o: Ph3P HOC CH₂ CH3 CH3 Yo. CH3 H3C CH3
Arrow-pushing Instructions IIn O: :CI: Step 2 CH3 H3C H CH3 Next〉 (1 of 1) Recheck
Draw curved arrows for the following reaction step. Arrow-pushing Instructions OX H-O-H ipt CH3 H3C-c-ci: Visited CH3 CH3 H3C/C+ CH3 + CI: 1 pt 1 pt Submit Answer Try Another Version 10 Item attempts remaining
Draw curved arrows to show electron reorganization for the reaction step below. Arrow-pushing Instructions no-X H3C-¢¢-H + :ö-H - H3c-=c-H + H-ö-H HH HH Draw curved arrows to show electron reorganization for the reaction step below. Arrow-pushing Instructions no XT H₂C 8 H₃C H3C—C—CH3 H3C—C—CH3 + H2O
name the alkane
Interactive 3D display mode o Hoc H, H, C-CH3 H3C CH CHHA 1 NO? H сн, сн, Spell out the full name of the compound. 6-ethyl-3,4-dimethyoctane
Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions IIn CH3 CH3 :0% H2O CH HaC CH3 H3C CH3
CH3NH2 CH3 CH3 ??? unsaturated aldehyde or ketone. Draw curved arrows to show he movement o electrons in this step o the reaction med ans m Nucleophiles such as amines can add to the ? carbon ofan a Arrow-pushing Instructions CH CH3 H3C H3C
Draw curved arrows to show electron reorganization for the reaction step below. Arrow-pushing Instructions no XT H3C-C-CH3 + I-2-1 :N-H :o: H3c-c-öchs + NH3
RE klon 1 1 pt CH3 CH3 H₂O - H30* + cm ution 2 stion 3 stion 4 pt 18 1 pt H3C-¢-CI CH3 H3C---OH CH3 estion 5 1 pt 2-chloro-2-methylpropane reacts with water in three steps to yield 2-methylpropan-2-ol. One of these steps is shown below, add curved arrows to the mechanism to indicate the movement of electrons in this step. estion 6 1pt Arrow-pushing Instructions Question 7 1 pt Question 8 Question Question 10 1 pt pt pe...
H3 C H2Br Br2, H30* HC X CH3 HzC CH3 H3C CH3 Aldehydes and ketones can be halogenated at their a-position by reaction with Cl, Br, or 12, under acidic conditions. Using Br2 under acidic conditions, an intermediate enol is formed which adds bromine at the a-position. The reaction stops after the addition of one bromine because the electron-withdrawing halogen decreases the basicity of the carbonyl oxygen, making the protonation less favorable. Not started curved arrows to show the movement...
(Review Topics 1. Hg(OAC)2, H20 2. NaBH, . H2O OH CHI CH3 H3C H3C Hoc Acid-catalyzed addition of water to an alkene yields an alcohol with Markovnikov repiochemistry. The electrophilic adds to the sp? carbon with the most hydrogens to yield the most stable carbocation intermediate, which then adds water to give the product alcohol Because a carbocation intermediate is formed, rearrangements can occur prior to the addition of water To avoid the possibility of rearrangement and still give a...