Specify the reagent you would use in each step of the following synthesis: OH step 1 step 2 HO Reagents Available a. LIAIH4 f. PBr3 k. CH3CH,MgBr b. H2SO4 g. Dess-Martin periodinane (DMP) 1. CgHgMgBr (phenylmagnesium bromide) c. HCI h. NaH m. (CH3)2CHMGB. d. HBr i. NaOH n. Cro3 e. SOCI, j. CH3M9B Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2|
Analyzing Infrared Spectra
The electromagnetic radiation or frequency is classified into radio-waves, micro-waves, infrared, visible, ultraviolet, X-rays and gamma rays. The infrared spectra emission refers to the portion between the visible and the microwave areas of electromagnetic spectrum. This spectral area is usually divided into three parts, near infrared (14,290 – 4000 cm-1), mid infrared (4000 – 400 cm-1), and far infrared (700 – 200 cm-1), respectively. The number set is the number of the wave (cm-1).
IR Spectrum Of Cyclohexanone
It is the analysis of the structure of cyclohexaone using IR data interpretation.
IR Spectrum Of Anisole
Interpretation of anisole using IR spectrum obtained from IR analysis.
IR Spectroscopy
Infrared (IR) or vibrational spectroscopy is a method used for analyzing the particle's vibratory transformations. This is one of the very popular spectroscopic approaches employed by inorganic as well as organic laboratories because it is helpful in evaluating and distinguishing the frameworks of the molecules. The infra-red spectroscopy process or procedure is carried out using a tool called an infrared spectrometer to obtain an infrared spectral (or spectrophotometer).
![**Specify the reagent you would use in each step of the following synthesis:**
**Reaction Scheme:**
- **Starting Material:** Displayed as a structure with a hydroxyl group (OH) and a hydrocarbon chain.
- **Step 1:** Some transformation occurs.
- **Step 2:** Another transformation leads to a new structure with an additional hydrocarbon chain and hydroxyl group (OH).
**Reagents Available:**
a. LiAlH₄
b. H₂SO₄
c. HCl
d. HBr
e. SOCl₂
f. PBr₃
g. Dess-Martin periodinane (DMP)
h. NaH
i. NaOH
j. CH₃MgBr
k. CH₃CH₂MgBr
l. C₆H₅MgBr (phenylmagnesium bromide)
m. (CH₃)₂CHMgBr
n. CrO₃
**Instructions:**
Write the letters of the reagents in the boxes below.
- **Reagent for step 1: [ ]**
- **Reagent for step 2: [ ]**
Complete the selection based on the specific transformations required in each step of the synthesis pathway.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F13f99433-34aa-4e92-8117-34b0d2272faf%2F3949d24f-8334-4fdf-9074-543eafeea320%2Fiss5ngq_processed.png&w=3840&q=75)
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