N each reaction box. place the best reagent and conditions from the list below. [Solved]

In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In every response field, place one of the best reagent and situations from
the listing under. (Some reagents could also be used greater than as soon as.)

Therapy of (Z)-pent-2-ene with molecule kinds a bridged bromonium ion adopted by the nucleophilic assault of , the bromonium ion ring opens after which lack of proton takes place to type two bromohydrin merchandise.

Ideas and motive
The idea used to resolve this downside is through the use of the given reagents, doable merchandise will likely be fashioned in every step after which label it precisely within the given containers as a way to type the precise product.
Right here, the beginning reactant is propylene and the ultimate product is epoxide.

Discount of triple bond.

Sodium hydride () is used as base, which summary the proton.
Hydroboration within the presence of tetrahydrofuran adopted by the oxidation offers a major alcohol.
Addition of to the double bond kinds a halohydrin product.
Sodium borohydride is used as a decreasing agent for the conversion of aldehyde to major alcohol and ketone to secondary alcohol.
Discount of alkyne with within the presence of Lindlars catalyst offers cis alkene. Equally, the trans alkene is fashioned with within the presence of .

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Step 3 of 5

The most effective reagents which are used on this response are as follows:

Therapy of propylene ion with a robust base, sodium hydride, kinds prop-1-yn-1-ide.
Right here, sodium hydride removes the proton from extra acidic carbon atom.
This prop-1-yn-1-ide ion acts as a robust nucleophile.

Be sure that the bonds to the extra substituted carbon atom however to not the much less substituted carbon atom.

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Br, and H,0
NH,(1)
NaH H3C2C=C-H H3C- C= prop-1-yne prop-1-yn-1-ide
H3cc=c: LO prop-1-yn-1-ide CH3CH2Br 123 H3C-c=c-CH2-CH3 pent-2-yne
H3C CEO-CH2-CH, H2, Lindlars catalyst C pent-2-yne H3C CH2-CH3 (Z)-pent-2-ene
OH Br2 2011!||| Illino HO H3C CH2 CH3 H3C CH2-CH3 Hac I CH2-CH3 Br (Z)-pent-2-ene (2R,3R)-2-bromopentan-3-ol (2R,3R)-3-bromopentan-2-ol
H OH I I 11 2.111111 T . C- C H3C CH2-CH3 H3C CH2-CH3 (2R,3R)-2-bromopentan-3-ol (2R,3R)-3-bromopentan-2-ol NaH IH |- liit. H3C CH2-CH3 (2S,3R)-2-ethyl-3-methyloxirane H3C CH2-CH3 (2R,3S)-2-ethyl-3-methyloxirane
NaH 1) 2) CH2CH2Br w H3C-EC-H H3C -CH3 Hzc V CH3 3) 4) 5) Hz, Lindlars Catalyst Br2, H20 Nah
NaH 1) 2) CH2CH2Br w H3C-EC-H H3C -CH3 Hzc V CH3 3) 4) 5) Hz, Lindlars Catalyst Br2, H20 Nah
We have been unable to transcribe this picture
In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.)

The most effective reagents which are used on this response are as follows:

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Step 3 of 5

Be sure that the nucleophilic substitution takes place on this response however not elimination.

Reply solely

The most effective reagents which are used on this response are as follows:

Therapy of propylene ion with a robust base, sodium hydride, kinds prop-1-yn-1-ide.
Right here, sodium hydride removes the proton from extra acidic carbon atom.
This prop-1-yn-1-ide ion acts as a robust nucleophile.

The most effective reagents which are used on this response are as follows:

Step 5 of 5

The most effective reagents which are used on this response are as follows:

Therapy of pent-2-yne with within the presence of Lindlars catalyst offers (Z)-pent-2-ene. Right here, cis alkene is fashioned.

Discount of triple bond.

Therapy of fashioned bromohydrin merchandise with a robust base, NaH, kinds the specified compounds.
The bottom abstracts the proton from the -OH group and kinds an oxyanion, which assaults the electrophilic carbon having leaving group and kinds the required compounds.

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Reply

The most effective reagents which are used on this response are as follows:

Be sure that the bonds to the extra substituted carbon atom however to not the much less substituted carbon atom.

Therapy of fashioned bromohydrin merchandise with a robust base, NaH, kinds the specified compounds.
The bottom abstracts the proton from the -OH group and kinds an oxyanion, which assaults the electrophilic carbon having leaving group and kinds the required compounds.

Step 5 of 5

Be sure that the bonds to the extra substituted carbon atom however to not the much less substituted carbon atom.

Therapy of fashioned bromohydrin merchandise with a robust base, NaH, kinds the specified compounds.
The bottom abstracts the proton from the -OH group and kinds an oxyanion, which assaults the electrophilic carbon having leaving group and kinds the required compounds.

Be sure that the bonds to the extra substituted carbon atom however to not the much less substituted carbon atom.

Br, and H,0
NH,(1)
NaH H3C2C=C-H H3C- C= prop-1-yne prop-1-yn-1-ide
H3cc=c: LO prop-1-yn-1-ide CH3CH2Br 123 H3C-c=c-CH2-CH3 pent-2-yne
H3C CEO-CH2-CH, H2, Lindlars catalyst C pent-2-yne H3C CH2-CH3 (Z)-pent-2-ene
OH Br2 2011!||| Illino HO H3C CH2 CH3 H3C CH2-CH3 Hac I CH2-CH3 Br (Z)-pent-2-ene (2R,3R)-2-bromopentan-3-ol (2R,3R)-3-bromopentan-2-ol
H OH I I 11 2.111111 T . C- C H3C CH2-CH3 H3C CH2-CH3 (2R,3R)-2-bromopentan-3-ol (2R,3R)-3-bromopentan-2-ol NaH IH |- liit. H3C CH2-CH3 (2S,3R)-2-ethyl-3-methyloxirane H3C CH2-CH3 (2R,3S)-2-ethyl-3-methyloxirane
NaH 1) 2) CH2CH2Br w H3C-EC-H H3C -CH3 Hzc V CH3 3) 4) 5) Hz, Lindlars Catalyst Br2, H20 Nah
NaH 1) 2) CH2CH2Br w H3C-EC-H H3C -CH3 Hzc V CH3 3) 4) 5) Hz, Lindlars Catalyst Br2, H20 Nah
We have been unable to transcribe this picture
In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.) In each reaction box, place the best reagent and conditions from
the list below. (Some reagents may be used more than once.)

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