How many of the reactions shown below (i-iii) would be expected to give the product shown as the majo product? i) NaOEt, HOEt OEt 1) KH, DMF ii) HS. 2) Br iii) 1 equivalent HI HO. O 2

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Chapter1: Chemical Foundations
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**Question:**

How many of the reactions shown below (i-iii) would be expected to give the product shown as the major product?

**Reaction Details:**

**i)** Cyclohexanone with an ethyl group is reacted with sodium ethoxide (NaOEt) and ethanol (HOEt) to form a compound with adjacent hydroxyl (OH) and ethoxy (OEt) groups on a cyclohexane ring.

**ii)** A thiol group (HS) attached to a butyl chain reacts with 1) potassium hydride (KH) in dimethylformamide (DMF), followed by 2) 1-bromo-2-methylpropane, resulting in a sulfide with an extended alkyl chain.

**iii)** A cyclic ether reacts with one equivalent of hydroiodic acid (HI) to produce a primary iodide and an alcohol in a six-carbon chain.

**Options:**
- ○ 3
- ○ 1
- ○ 2
- ○ 0

The question asks to determine how many of these reactions correctly result in the depicted major product.
Transcribed Image Text:**Question:** How many of the reactions shown below (i-iii) would be expected to give the product shown as the major product? **Reaction Details:** **i)** Cyclohexanone with an ethyl group is reacted with sodium ethoxide (NaOEt) and ethanol (HOEt) to form a compound with adjacent hydroxyl (OH) and ethoxy (OEt) groups on a cyclohexane ring. **ii)** A thiol group (HS) attached to a butyl chain reacts with 1) potassium hydride (KH) in dimethylformamide (DMF), followed by 2) 1-bromo-2-methylpropane, resulting in a sulfide with an extended alkyl chain. **iii)** A cyclic ether reacts with one equivalent of hydroiodic acid (HI) to produce a primary iodide and an alcohol in a six-carbon chain. **Options:** - ○ 3 - ○ 1 - ○ 2 - ○ 0 The question asks to determine how many of these reactions correctly result in the depicted major product.
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